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: rs2948294
rs2948294
2 8 8237439 intron variant A/G snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs2980478
rs2980478
2 8 8230708 intron variant T/A;C snv 0.700 1.000 1 2017 2017