RS10936599 MYNN

Health Risk Chr 3:169774312 snv missense variant
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What This Variant Does
"[GWAS:Celiac disease]"
Associated Conditions
GWAS Studies (17)
Trait Risk Allele OR / Beta P-value Study
Telomere length 8E-95 PubMed
Telomere length T β: 0.097 3E-31 PubMed
Lymphoid neoplasms (somatic mutation group 2 phenocluster) OR: 0.85 2E-23 PubMed
Uterine fibroids T β: 0.095 3E-21 PubMed
Cutaneous melanoma (MTAG) C β: 0.072 8E-19 PubMed
eosinophil (fraction, maximum, inv-norm transformed) C β: 0.03 1E-17 PubMed
eosinophil (absolute count, mean, inv-norm transformed) C β: 0.033 2E-17 PubMed
Multiple myeloma G OR: 1.26 9E-14 PubMed
Colorectal cancer T β: 0.053 1E-13 PubMed
Chronic lymphocytic leukemia C OR: 1.26 2E-9 PubMed
Bladder cancer C OR: 1.18 5E-9 PubMed
Colorectal cancer C OR: 1.04 3E-8 PubMed
Multiple myeloma C OR: 1.16 3E-8 PubMed
Celiac disease A OR: 1.12 5E-7 PubMed
Multiple sclerosis G OR: 1.1 7E-7 PubMed
Colorectal cancer C OR: 1.06 2E-6 PubMed
Colorectal cancer C OR: 1.06 9E-6 PubMed
Population Frequencies
gnomAD ALL
74.1%
1kG AFR
3.7%
1kG ALL
27.1%
1kG AMR
35.4%
1kG EAS
42.2%
1kG EUR
24.3%
1kG SAS
23.8%
Ask Dr. Hemsworth about this variant