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rs80357170(A;C)

From SNPedia
BRCA1 variant of uncertain significance for breast cancer
Is agenotype
ofrs80357170
GeneBRCA1
Chromosome17
Position43,092,854
mentionedby
Magnitude1
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 1 BRCA1 variant of uncertain significance for breast cancer
(A;T) 6 BRCA1 variant considered pathogenic for breast cancer

see details via ClinVar sidebar/box on associated SNP/rs# page