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: rs121917835
rs121917835
3 0.878 0.036 8 22164010 missense variant T/A snp 0.010 1.000 1 2008 2008
dbSNP: rs35705950
rs35705950
7 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.030 1.000 3 2011 2016
dbSNP: rs762396570
rs762396570
2 0.923 0.071 8 22163500 missense variant G/C snp 0.010 1.000 1 2015 2015