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: rs3802842
rs3802842
25 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012
dbSNP: rs4779584
rs4779584
16 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 0.010 1.000 1 2012 2012
dbSNP: rs6691170
rs6691170
12 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 0.010 1.000 1 2012 2012