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: rs121913529
rs121913529
19 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.820 1.000 8 2005 2019
dbSNP: rs112445441
rs112445441
8 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.810 1.000 0 2015 2015
dbSNP: rs121913530
rs121913530
11 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.810 1.000 0 2007 2012
dbSNP: rs17851045
rs17851045
15 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 0.700 0