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: rs13224557
rs13224557
1 7 69911737 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs941346
rs941346
1 7 70789688 intron variant G/T snv 0.60 0.700 1.000 1 2019 2019