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: rs1142345
rs1142345
9 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs79050301
rs79050301
1 1.000 0.120 6 18151959 intron variant T/C snv 4.5E-02 0.700 1.000 1 2018 2018