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: rs1006737
rs1006737
31 0.679 0.107 12 2236129 intron variant G/A snp 0.37 0.010 1.000 1 2010 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: rs10410544
rs10410544
3 0.878 0.107 19 38894892 intron variant T/C snp 0.68 0.66 0.010 1.000 1 2014 2014
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: rs1049353
rs1049353
26 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 0.010 1.000 1 2012 2012
dbSNP: rs1082214
rs1082214
MIP
5 0.923 0.071 12 56452706 non coding transcript exon variant C/T snp 8.4E-02 0.010 1.000 1 2010 2010
dbSNP: rs10848635
rs10848635
2 0.923 0.071 12 2207029 intron variant T/A snp 0.35 0.010 1.000 1 2010 2010
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: rs11111
rs11111
4 0.878 0.071 5 37814000 3 prime UTR variant T/C snp 0.21 0.010 1.000 1 2014 2014
dbSNP: rs11636753
rs11636753
3 0.878 0.107 15 78636604 intron variant G/T snp 0.36 0.010 1.000 1 2012 2012
dbSNP: rs11754661
rs11754661
5 0.846 0.107 6 150885942 intron variant G/A,T snp 4.9E-02 0.010 1.000 1 2016 2016
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: rs1187329
rs1187329
2 0.923 0.071 9 84674365 intron variant A/G snp 0.53 0.010 1.000 1 2010 2010
dbSNP: rs11904814
rs11904814
3 0.923 0.071 2 207562074 intron variant T/G snp 0.31 0.010 1.000 1 2010 2010
dbSNP: rs11911834
rs11911834
3 0.878 0.071 21 46602608 5 prime UTR variant G/A,T snp 6.4E-05; 5.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs120074175
rs120074175
4 0.846 0.071 12 72031544 missense variant G/A snp 1.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs1202184
rs1202184
6 0.846 0.107 7 87584585 intron variant C/T snp 0.41 0.010 1.000 1 2011 2011
dbSNP: rs12137417
rs12137417
2 0.923 0.071 1 231950407 intron variant G/A snp 0.17 0.010 1.000 1 2012 2012
dbSNP: rs12150214
rs12150214
2 0.923 0.071 17 30223870 intron variant C/G,T snp 0.75 0.010 1.000 1 2010 2010
dbSNP: rs12229394
rs12229394
3 0.923 0.071 12 71999134 intron variant G/A snp 0.29 0.010 1.000 1 2010 2010
dbSNP: rs1229984
rs1229984
50 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 0.010 < 0.001 1 2015 2015
dbSNP: rs1256049
rs1256049
21 0.679 0.429 14 64257333 synonymous variant C/T snp 6.7E-02 7.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs12912233
rs12912233
3 0.878 0.071 15 60974897 intron variant C/T snp 0.38 0.010 1.000 1 2011 2011
dbSNP: rs12936511
rs12936511
4 0.923 0.071 17 45807036 synonymous variant C/T snp 3.1E-02 3.1E-02 0.010 1.000 1 2009 2009
dbSNP: rs1325757098
rs1325757098
TAT
3 0.878 0.071 16 71576223 missense variant C/T snp 8.0E-06 0.010 1.000 1 2018 2018