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: rs4428528
rs4428528
1 1.000 0.080 6 32462585 intron variant C/G snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs7746922
rs7746922
2 0.925 0.200 6 32463198 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7766843
rs7766843
2 0.925 0.200 6 32462952 intron variant C/T snv 0.29 0.700 1.000 1 2009 2009
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 2009 2009
dbSNP: rs9268853
rs9268853
10 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs9268856
rs9268856
6 0.807 0.240 6 32461942 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9268858
rs9268858
5 0.882 0.200 6 32461981 intron variant T/C snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs9268877
rs9268877
5 0.827 0.200 6 32463370 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9268878
rs9268878
2 0.925 0.200 6 32463515 intron variant T/A snv 0.29 0.700 1.000 1 2009 2009