RS16942 BRCA1

Health Risk Chr 17:43091982 snv missense variant
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What This Variant Does
"This SNP, a variant in the BRCA1 gene, is 1 of 25 SNPs reported to represent independently minor, bu...
Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Aspartate aminotransferase levels C β: 0.018 1E-12 PubMed
Population Frequencies
gnomAD ALL
0%
1kG AFR
78.2%
1kG ALL
35.3%
1kG AMR
37.5%
1kG EAS
62.9%
1kG EUR
64.5%
1kG SAS
50.2%
Other Variants in BRCA1
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