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: rs1008833
rs1008833
3 1 204457167 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs12092943
rs12092943
1 1 204465799 intron variant T/G snv 0.22 0.700 1.000 1 2018 2018