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: rs7486220
rs7486220
2 0.923 0.071 12 56443632 intron variant snp 0.010 1.000 1 2010 2010
dbSNP: rs2522833
rs2522833
6 0.821 0.071 7 82824392 missense variant A/C snp 0.45 0.35 0.040 0.750 4 2010 2015
dbSNP: rs1176744
rs1176744
16 0.715 0.143 11 113932306 missense variant A/C snp 0.33 0.34 0.010 1.000 1 2008 2008
dbSNP: rs1881457
rs1881457
7 0.801 0.214 5 132656717 intron variant A/C snp 0.22 0.010 < 0.001 1 2014 2014
dbSNP: rs1935062
rs1935062
3 0.878 0.071 13 105475787 intron variant A/C snp 0.34 0.010 < 0.001 1 2010 2010
dbSNP: rs2619522
rs2619522
5 0.846 0.071 6 15653418 intron variant A/C snp 0.25 0.010 1.000 1 2011 2011
dbSNP: rs7296288
rs7296288
DHH
4 0.846 0.071 12 49086185 regulatory region variant A/C snp 0.52 0.010 1.000 1 2016 2016
dbSNP: rs14259
rs14259
15 0.734 0.321 12 121915890 missense variant A/C,G snp 4.0E-06; 0.32 0.26 0.010 1.000 1 2013 2013
dbSNP: rs2072115
rs2072115
4 0.878 0.071 12 47751585 intron variant A/C,G snp 3.2E-05; 0.23 0.010 1.000 1 2010 2010
dbSNP: rs4713916
rs4713916
6 0.846 0.107 6 35702206 intron variant A/C,G,T snp 0.77 0.010 1.000 1 2006 2006
dbSNP: rs746532397
rs746532397
2 0.923 0.071 19 10420895 missense variant A/C,T snp 1.5E-05 0.010 1.000 1 2007 2007
dbSNP: rs9340799
rs9340799
37 0.611 0.607 6 151842246 intron variant A/G snp 0.31 0.030 1.000 3 2011 2018
dbSNP: rs2230912
rs2230912
10 0.769 0.143 12 121184393 missense variant A/G snp 0.13 0.12 0.020 1.000 2 2009 2010
dbSNP: rs1013940
rs1013940
3 0.878 0.071 2 107992192 missense variant A/G snp 9.3E-02 7.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs10434
rs10434
8 0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59 0.010 1.000 1 2015 2015
dbSNP: rs11030104
rs11030104
6 0.878 0.071 11 27662970 intron variant A/G snp 0.16 0.010 1.000 1 2016 2016
dbSNP: rs1187329
rs1187329
2 0.923 0.071 9 84674365 intron variant A/G snp 0.53 0.010 1.000 1 2010 2010
dbSNP: rs139315125
rs139315125
6 0.846 0.071 1 7809900 missense variant A/G snp 5.6E-03 8.2E-03 0.010 1.000 1 2016 2016
dbSNP: rs1799971
rs1799971
57 0.611 0.500 6 154039662 missense variant A/G snp 0.19 0.12 0.010 1.000 1 2016 2016
dbSNP: rs1801394
rs1801394
60 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 0.010 1.000 1 2014 2014
dbSNP: rs1805087
rs1805087
MTR
75 0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 0.010 1.000 1 2009 2009
dbSNP: rs2075650
rs2075650
27 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 0.010 1.000 1 2014 2014
dbSNP: rs2253206
rs2253206
3 0.923 0.071 2 207527254 intron variant A/G snp 0.47 0.010 1.000 1 2011 2011
dbSNP: rs334558
rs334558
11 0.744 0.107 3 120094435 regulatory region variant A/G snp 0.52 0.010 1.000 1 2012 2012
dbSNP: rs4906902
rs4906902
5 0.821 0.143 15 26774621 intron variant A/G snp 0.15 0.010 1.000 1 2012 2012