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: rs104894057
rs104894057
1 1.000 0.080 7 19116966 missense variant T/G snv 0.800 1.000 3 1997 2001