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: rs10815466
rs10815466
2 1.000 9 680714 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs73639400
rs73639400
2 1.000 9 683423 intron variant T/C snv 0.35 0.700 1.000 1 2018 2018