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: rs1058172
rs1058172
4 0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 0.700 1.000 1 2014 2014
dbSNP: rs1065852
rs1065852
19 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 0.700 1.000 1 2014 2014