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: rs4944940
rs4944940
9 0.790 0.080 11 74704207 intron variant G/A;T snv 3.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs61389091
rs61389091
10 0.776 0.080 11 74716876 intron variant C/G;T snv 0.700 1.000 1 2019 2019