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: rs121913469
rs121913469
11 0.763 0.240 17 39723966 missense variant TT/CC mnv 0.710 1.000 2 2004 2015
dbSNP: rs372043866
rs372043866
18 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 0.030 1.000 3 2006 2016
dbSNP: rs1057519857
rs1057519857
4 0.882 0.080 17 39724772 missense variant T/C snv 0.010 1.000 1 2015 2015
dbSNP: rs1058808
rs1058808
27 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 1.000 1 2008 2008
dbSNP: rs1196929947
rs1196929947
3 0.882 0.080 17 39723351 missense variant G/A snv 0.010 1.000 1 2018 2018