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: rs1057519789
rs1057519789
1 1.000 0.080 1 162775707 missense variant A/G;T snv 4.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs1057519790
rs1057519790
1 1.000 0.080 1 162778617 missense variant G/T snv 0.700 1.000 1 2011 2011
dbSNP: rs144594252
rs144594252
3 0.882 0.080 1 162754625 missense variant C/G snv 6.8E-05 5.6E-05 0.700 1.000 1 2011 2011
dbSNP: rs376303676
rs376303676
1 1.000 0.080 1 162759881 missense variant G/A;T snv 8.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs578015216
rs578015216
1 1.000 0.080 1 162759840 missense variant T/C;G snv 2.8E-05 0.700 1.000 1 2011 2011
dbSNP: rs201701502
rs201701502
5 0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 0.010 1.000 1 2017 2017