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: rs104894647
rs104894647
2 0.925 0.080 17 72122804 missense variant A/G snv 0.700 0
dbSNP: rs137853128
rs137853128
2 0.925 0.080 17 72121618 missense variant C/A snv 0.700 0
dbSNP: rs28940282
rs28940282
2 0.925 0.080 17 72122780 missense variant C/T snv 0.700 0