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: rs121913355
rs121913355
4 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs121913361
rs121913361
1 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 0
dbSNP: rs121913370
rs121913370
1 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 0