RS1801516 Unknown gene

Other Chr 11:108304735
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What This Variant Does
"This SNP lies within the gene coding for ATM (Ataxia telegensia mutated), a main role of which is th...
GWAS Studies (7)
Trait Risk Allele OR / Beta P-value Study
Cutaneous malignant melanoma G OR: 1.14 2E-21 PubMed
Nevus count or cutaneous melanoma G 4E-21 PubMed
Melanoma OR: 1.19 3E-9 PubMed
Melanoma OR: 1.14 3E-9 PubMed
Aspartate aminotransferase levels A β: 0.02 6E-9 PubMed
Uterine fibroids G OR: 1.1 7E-8 PubMed
Melanoma OR: 0.81 1E-7 PubMed
Ask Dr. Hemsworth about this variant