Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202179

From SNPedia

ClinVar
Risk rs786202179(;)
Alt rs786202179(;)
Reference rs786202179(CGGCTTTCCCCGTGAA;CGGCTTTCCCCGTGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33445583_33445598del16
CLNSRC
CLNACC RCV000164875.1,