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: rs10079250
rs10079250
7 0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 0.010 1.000 1 2017 2017
dbSNP: rs140461341
rs140461341
2 6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 0.010 1.000 1 2017 2017