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
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.800 0.857 28 2007 2017
dbSNP: rs16901979
rs16901979
17 0.724 0.480 8 127112671 intron variant C/A snv 0.16 0.800 0.950 20 2007 2018
dbSNP: rs6983561
rs6983561
3 0.925 0.080 8 127094635 intron variant A/C snv 0.17 0.780 1.000 9 2008 2017
dbSNP: rs16901966
rs16901966
3 0.925 0.080 8 127098007 intron variant A/G snv 0.13 0.730 1.000 5 2008 2016
dbSNP: rs620861
rs620861
3 0.925 0.080 8 127323428 intron variant G/A snv 0.36 0.730 0.750 4 2008 2017
dbSNP: rs1456315
rs1456315
9 0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 0.720 1.000 6 2010 2014
dbSNP: rs7837328
rs7837328
8 0.882 0.120 8 127410882 intron variant A/G snv 0.52 0.720 1.000 4 2008 2014
dbSNP: rs13254738
rs13254738
8 0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv 0.720 0.667 3 2008 2012
dbSNP: rs16902094
rs16902094
3 0.882 0.160 8 127308101 intron variant A/G snv 0.15 0.720 1.000 3 2009 2017
dbSNP: rs7014346
rs7014346
14 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.710 1.000 3 2008 2015
dbSNP: rs1016343
rs1016343
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.700 1.000 4 2008 2013
dbSNP: rs445114
rs445114
3 0.882 0.160 8 127310936 intron variant T/A;C snv 0.700 1.000 3 2009 2013
dbSNP: rs10505477
rs10505477
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 2 2008 2013
dbSNP: rs10505483
rs10505483
2 0.925 0.080 8 127112950 intron variant C/T snv 0.16 0.700 1.000 2 2008 2012
dbSNP: rs16901970
rs16901970
1 1.000 0.080 8 127100470 intron variant T/G snv 0.13 0.700 1.000 2 2008 2012
dbSNP: rs7817677
rs7817677
1 1.000 0.080 8 127113259 intron variant A/G snv 0.13 0.700 1.000 2 2008 2012
dbSNP: rs10808556
rs10808556
2 0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 0.700 1.000 1 2008 2008
dbSNP: rs12543663
rs12543663
1 1.000 0.080 8 126912414 intron variant C/A;T snv 0.700 1.000 1 2008 2008
dbSNP: rs13252298
rs13252298
8 0.827 0.160 8 127082911 non coding transcript exon variant A/G snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs1378897
rs1378897
2 0.925 0.080 8 127110414 intron variant C/T snv 5.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs1456306
rs1456306
2 0.925 0.080 8 127104255 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs13281615
rs13281615
18 0.716 0.360 8 127343372 intron variant A/G snv 0.43 0.020 1.000 2 2008 2009
dbSNP: rs188140481
rs188140481
4 0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 0.020 1.000 2 2015 2015
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: rs116041037
rs116041037
2 0.925 0.080 8 127119564 intron variant G/A snv 1.0E-02 0.010 1.000 1 2015 2015