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: rs1780329
rs1780329
2 0.925 0.200 1 21576457 intron variant C/A snv 0.25 0.010 1.000 1 2007 2007
dbSNP: rs3738099
rs3738099
1 1.000 0.040 1 21568242 missense variant T/A;C snv 0.010 1.000 1 2007 2007
dbSNP: rs3767155
rs3767155
1 1.000 0.040 1 21558702 intron variant C/A;G;T snv 0.010 1.000 1 2007 2007