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: rs2062432
rs2062432
4 3 123359232 intron variant G/A snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs7614016
rs7614016
2 3 123351579 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018