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: rs28457693
rs28457693
1 9 95455066 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs28510415
rs28510415
1 9 95482744 non coding transcript exon variant A/G snv 6.7E-02 0.700 1.000 1 2016 2016