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: rs397517096
rs397517096
EGFR
4 0.851 0.120 7 55174776 missense variant TT/CC mnv 0.010 1.000 1 2015 2015