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: rs25490
rs25490
XRCC1
4 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 0.010 1.000 1 2014 2014