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: rs1057518083
rs1057518083
21 0.851 0.120 14 101986552 missense variant C/T snv 0.700 0
dbSNP: rs1057518946
rs1057518946
8 0.882 0.080 X 71223816 missense variant G/T snv 0.700 0
dbSNP: rs121908457
rs121908457
13 0.882 0.120 5 137870815 missense variant C/T snv 0.700 0
dbSNP: rs763944786
rs763944786
5 0.925 0.080 19 38469119 missense variant C/T snv 1.2E-05 1.4E-05 0.700 0