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: rs1047781
rs1047781
11 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs492602
rs492602
7 0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 0.700 1.000 1 2017 2017
dbSNP: rs602662
rs602662
16 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 0.700 1.000 1 2015 2015
dbSNP: rs679574
rs679574
7 0.827 0.120 19 48702851 intron variant C/G snv 0.45 0.700 1.000 1 2016 2016