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: rs112445441
rs112445441
8 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 16 2005 2015
dbSNP: rs121913529
rs121913529
19 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 12 2005 2014
dbSNP: rs17851045
rs17851045
15 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 0.700 1.000 12 2005 2016
dbSNP: rs121913530
rs121913530
11 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.700 1.000 11 2005 2014
dbSNP: rs121913238
rs121913238
3 0.732 0.240 12 25227343 missense variant G/C;T snv 0.700 1.000 9 2005 2014
dbSNP: rs121913240
rs121913240
6 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 1.000 9 2005 2014
dbSNP: rs121913535
rs121913535
5 0.742 0.320 12 25245348 missense variant C/A;G;T snv 0.700 1.000 9 2005 2014
dbSNP: rs770248150
rs770248150
6 0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 0.700 1.000 9 2005 2016
dbSNP: rs1057519725
rs1057519725
2 0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 0.700 1.000 8 2005 2011
dbSNP: rs121913527
rs121913527
2 0.807 0.320 12 25225628 missense variant C/A;G;T snv 0.700 1.000 8 2005 2011
dbSNP: rs121913528
rs121913528
11 0.851 0.160 12 25227349 missense variant C/A;T snv 0.700 1.000 2 2011 2014
dbSNP: rs121913236
rs121913236
1 0.882 0.160 12 25245321 missense variant G/C;T snv 0.700 1.000 1 2014 2014