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: rs4987188
rs4987188
11 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 0.010 < 0.001 1 2017 2017
dbSNP: rs63750875
rs63750875
15 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 0.010 1.000 1 2003 2003
dbSNP: rs730881756
rs730881756
2 0.925 0.080 2 47445653 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2015 2015