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: rs121913293
rs121913293
18 0.732 0.360 10 87952142 missense variant C/A;T snv 0.700 1.000 5 2007 2017
dbSNP: rs147232392
rs147232392
3 0.882 0.240 X 137566740 missense variant G/A;T snv 2.6E-03 0.700 1.000 1 1990 1990
dbSNP: rs121909231
rs121909231
32 0.667 0.600 10 87961095 stop gained C/A;T snv 0.700 0
dbSNP: rs1224040268
rs1224040268
12 0.742 0.360 10 87931091 splice donor variant T/A;C snv 7.0E-06 0.700 0
dbSNP: rs370795352
rs370795352
13 0.742 0.360 10 87933163 missense variant T/A;C snv 4.0E-06 0.700 0
dbSNP: rs398122850
rs398122850
1 1.000 0.200 X 137566853 inframe insertion -/GCCGCC delins 0.700 0
dbSNP: rs863224909
rs863224909
14 0.732 0.360 10 87960952 stop gained C/A;G snv 0.700 0