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: rs1109151
rs1109151
1 22 41356940 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs5758297
rs5758297
2 22 41324693 intron variant A/G snv 0.41 0.700 1.000 1 2016 2016