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: rs12720356
rs12720356
12 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs35018800
rs35018800
9 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 0.700 1.000 1 2016 2016