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: rs4851221
rs4851221
1 2 99663560 intron variant G/A snv 0.85 0.700 1.000 2 2018 2019
dbSNP: rs9678859
rs9678859
1 2 99672016 intron variant A/G snv 0.84 0.700 1.000 1 2019 2019