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: rs1983891
rs1983891
4 0.925 0.080 6 41568689 intron variant C/T snv 0.35 0.720 1.000 4 2010 2019
dbSNP: rs4245739
rs4245739
21 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 0.720 1.000 4 2013 2018
dbSNP: rs4962416
rs4962416
3 0.882 0.160 10 125008303 intron variant T/C snv 0.23 0.720 1.000 4 2008 2018
dbSNP: rs5945619
rs5945619
3 0.882 0.160 X 51498820 non coding transcript exon variant C/T snv 0.720 1.000 4 2008 2018
dbSNP: rs11672691
rs11672691
3 0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 0.720 0.667 3 2013 2018
dbSNP: rs11986220
rs11986220
2 0.925 0.080 8 127519444 intergenic variant A/G;T snv 0.720 1.000 3 2009 2015
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: rs13385191
rs13385191
4 0.925 0.080 2 20688505 intron variant A/G snv 0.20 0.720 1.000 3 2010 2014
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: rs188140481
rs188140481
4 0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 0.720 1.000 3 2012 2015
dbSNP: rs1512268
rs1512268
6 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 0.710 1.000 6 2009 2019
dbSNP: rs7931342
rs7931342
20 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 0.710 1.000 5 2008 2018
dbSNP: rs12621278
rs12621278
7 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.710 1.000 4 2009 2019
dbSNP: rs2660753
rs2660753
9 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 0.710 0.750 4 2008 2019
dbSNP: rs7127900
rs7127900
3 0.882 0.160 11 2212344 intergenic variant A/C;G snv 0.710 1.000 4 2009 2018
dbSNP: rs9364554
rs9364554
3 0.882 0.160 6 160412632 intron variant C/T snv 0.21 0.710 1.000 4 2008 2018
dbSNP: rs9600079
rs9600079
5 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 0.710 1.000 4 2010 2019
dbSNP: rs2242652
rs2242652
16 0.724 0.400 5 1279913 intron variant G/A snv 0.18 0.710 1.000 3 2011 2018
dbSNP: rs636291
rs636291
2 0.925 0.080 1 10496040 intron variant G/A snv 0.55 0.710 1.000 3 2014 2018
dbSNP: rs7837688
rs7837688
2 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 0.710 1.000 3 2010 2019
dbSNP: rs8102476
rs8102476
8 0.776 0.240 19 38244973 intron variant C/T snv 0.40 0.710 1.000 3 2009 2018
dbSNP: rs902774
rs902774
2 0.925 0.080 12 52880120 regulatory region variant G/A snv 0.12 0.710 1.000 3 2011 2018
dbSNP: rs11571833
rs11571833
43 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 0.710 1.000 2 2016 2016
dbSNP: rs116041037
rs116041037
2 0.925 0.080 8 127119564 intron variant G/A snv 1.0E-02 0.710 1.000 2 2015 2015
dbSNP: rs2292884
rs2292884
2 0.925 0.080 2 237534583 missense variant A/G snv 0.28 0.34 0.710 1.000 2 2011 2018