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: rs6903608
rs6903608
11 0.742 0.400 6 32460508 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9268831
rs9268831
4 0.851 0.280 6 32459971 non coding transcript exon variant C/T snv 0.54 0.51 0.700 1.000 1 2007 2007
dbSNP: rs9268832
rs9268832
4 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 0.700 1.000 1 2010 2010
dbSNP: rs9268853
rs9268853
10 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs9268858
rs9268858
5 0.882 0.200 6 32461981 intron variant T/C snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs9268877
rs9268877
5 0.827 0.200 6 32463370 intron variant A/G;T snv 0.700 1.000 1 2007 2007