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: rs59885338
rs59885338
4 0.851 0.120 1 156135268 missense variant C/T snv 3.6E-05 2.8E-05 0.730 1.000 3 2003 2008
dbSNP: rs142000963
rs142000963
8 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 0.700 1.000 2 2008 2014
dbSNP: rs57318642
rs57318642
4 0.851 0.200 1 156137203 missense variant C/T snv 1.4E-05 1.4E-05 0.700 0
dbSNP: rs60864230
rs60864230
7 0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs80356814
rs80356814
15 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 0.700 0
dbSNP: rs1057515421
rs1057515421
2 0.925 0.120 1 156136284 stop gained C/T snv 0.020 1.000 2 2003 2008