Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs267606998
rs267606998
RAD51C
1 1.000 17 58695159 missense variant G/T snv 0.800 1.000 3 2010 2014