Search

for
Search:

Did you mean Single Nucleotide Polymorphisms?

GlossarySingle Nucleotide Polymorphisms

variations in a single DNA building block among individuals

Single Nucleotide Polymorphisms (SNPs) are variations at a single position in a DNA sequence among individuals. These genetic differences can influence how people develop diseases, respond to pathogens, chemicals, drugs, and other substances, making them crucial for personalized medicine and genetic research.

Related Terms

Sort by

Research

30 / 1000+ results

research Association of single nucleotide polymorphisms in the RAB5B gene 3′UTR region with polycystic ovary syndrome in Chinese Han women

11 citations , April 2019 in “Bioscience Reports”

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

research Association of Single Nucleotide Polymorphisms in the CYP19A1 Gene with Female Pattern Hair Loss in a Chinese Population

7 citations , January 2015 in “Dermatology”

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

research Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology

2 citations , December 2024 in “Journal of Cosmetic Dermatology”

SNP profiling allows personalized skincare treatments for better results and fewer side effects.

research Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits

2 citations , May 2024 in “BMC Genomics”

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Single Nucleotide Polymorphisms Associated with Elevated Alanine Aminotransferase in Patients Receiving Asunaprevir Plus Daclatasvir Combination Therapy for Chronic Hepatitis C

research Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C

2 citations , July 2019 in “PLOS ONE”

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Genotypes of Single-Nucleotide Polymorphisms on DENND1A in Association with Polycystic Ovary Syndrome Among Saudi Arabian Females

research Genotypes of Single-nucleotide polymorphisms on DENND1A in an association with polycystic ovary syndrome among Saudi Arabian females

July 2025

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

research Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss

May 2025 in “Egyptian Journal of Dermatology and Venerology”

Certain gene changes and hormone levels are linked to female hair loss.

Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case-Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk

research Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk

January 2025 in “Nutrients”

Genetic factors and diet significantly increase the risk of male pattern baldness.

Genetic Single Nucleotide Polymorphisms of IL-16 and Its Concentration in Patients Infected with Alopecia Areata in Diyala Province, Iraq

research Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq

January 2023 in “International Journal of Zoological Investigations”

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

research [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].

June 2016 in “PubMed”

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

research The impact of certain genetic variants (single nucleotide polymorphisms) on incidence and severity of COVID‐19

7 citations , January 2021 in “The journal of gene medicine”

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

research Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †

1 citations , October 2025 in “Micromachines”

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

research Determining the Relationship Among Cattle Genotype, Hair Coat Score, and Productivity Through the Investigation of Single Nucleotide Polymorphisms within Prolactin, Dopamine Receptor D2, and Melatonin Receptor 1A

January 2019

research Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep

25 citations , April 2017 in “PloS one”

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

research Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer

23 citations , January 2014 in “International Journal of Biological Sciences”

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

research Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans

22 citations , January 2014 in “Journal of Interferon & Cytokine Research”

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Androgenetic Alopecia and Polymorphism of the Androgen Receptor Gene (SNP rs6152) in Patients with Benign Prostate Hyperplasia or Prostate Cancer

research Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer

11 citations , March 2014 in “Journal of The European Academy of Dermatology and Venereology”

Hair loss gene linked to prostate issues.

research Association between Polymorphisms of OCT1 and Metabolic Response to Metformin in Women with Polycystic Ovary Syndrome

11 citations , April 2019 in “International Journal of Molecular Sciences”

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

research Association between IL16 gene polymorphisms and susceptibility to alopecia areata in the Korean population

11 citations , December 2013 in “International Journal of Dermatology”

IL16 gene variations may affect the risk of alopecia areata in Koreans.

research The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata

9 citations , May 2019 in “Medicine”

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

research Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men

9 citations , September 2014 in “Cancer Epidemiology, Biomarkers & Prevention”

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

research Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population

8 citations , January 2015 in “Genetics and Molecular Research”

Certain gene variations increase the risk of alopecia areata in Koreans.

research Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)

5 citations , January 2016 in “Genetics and molecular research”

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

research Association between EGF and EGFR Gene Polymorphisms and Susceptibility to Alopecia Areata in the Korean Population

2 citations , January 2019 in “Annals of Dermatology”

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

research Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients

1 citations , October 2024 in “Medicina”

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

research Effects of KISS1 structural polymorphism on the risk of polycystic ovary syndrome and reproductive hormones in Iraqi women who take metformin

September 2023 in “Journal of International Medical Research”

Metformin increases FSH levels in PCOS, and KISS1 gene variations may influence PCOS development.

research Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease

September 2022 in “bioRxiv (Cold Spring Harbor Laboratory)”

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.