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: rs11066028
rs11066028
2 1.000 0.080 12 111807366 intron variant A/C snv 0.45 0.010 1.000 1 2018 2018
dbSNP: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2018 2018
dbSNP: rs7296651
rs7296651
2 0.925 0.160 12 111809150 intron variant C/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs886205
rs886205
8 0.827 0.360 12 111766623 intron variant A/G snv 0.35 0.010 1.000 1 2018 2018