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: rs6983267
rs6983267
55 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.800 0.871 24 2007 2019
dbSNP: rs620861
rs620861
2 0.925 0.080 8 127323428 intron variant G/A snv 0.36 0.030 0.667 3 2009 2017
dbSNP: rs13281615
rs13281615
17 0.716 0.360 8 127343372 intron variant A/G snv 0.43 0.020 1.000 2 2008 2009
dbSNP: rs7837328
rs7837328
8 0.882 0.120 8 127410882 intron variant A/G snv 0.52 0.020 1.000 2 2014 2014
dbSNP: rs10505474
rs10505474
3 0.925 0.080 8 127405259 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
dbSNP: rs7014346
rs7014346
5 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.010 1.000 1 2015 2015