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: rs747619345
rs747619345
ERCC2
2 0.925 0.240 19 45365151 missense variant G/A snv 8.0E-06 0.010 1.000 1 1999 1999