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: rs1462977
rs1462977
1 8 98103131 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs57392722
rs57392722
1 8 98115756 intron variant C/G;T snv 0.700 1.000 1 2018 2018