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: rs4988781
rs4988781
1 15 100260635 intron variant A/C snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs72755233
rs72755233
5 1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 0.700 1.000 1 2019 2019