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: rs10185199
rs10185199
1 2 40055062 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs985060
rs985060
1 2 40057790 intron variant G/A;T snv 0.700 1.000 1 2019 2019