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: rs12192704
rs12192704
1 1.000 0.120 6 30824493 intron variant G/A snv 0.11 0.700 1.000 2 2007 2009
dbSNP: rs4713391
rs4713391
1 1.000 0.120 6 30824458 intron variant T/C snv 0.12 0.700 1.000 2 2007 2009
dbSNP: rs4713380
rs4713380
5 0.925 0.120 6 30817496 intron variant T/C snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs4713385
rs4713385
5 0.925 0.120 6 30819816 intron variant G/A snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9295924
rs9295924
5 0.925 0.120 6 30814584 non coding transcript exon variant G/A snv 0.27 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9378109
rs9378109
5 0.925 0.120 6 30806697 intron variant C/A snv 0.16 0.700 1.000 1 2009 2009