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: rs1354034
rs1354034
5 3 56815721 intron variant T/C snp 0.52 0.800 6 2011 2017
dbSNP: rs210134
rs210134
2 6 33572432 intron variant A/G snp 0.73 0.800 5 2011 2016
dbSNP: rs3184504
rs3184504
55 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 0.800 3 2011 2017
dbSNP: rs6993770
rs6993770
6 8 105569300 intron variant A/T snp 0.30 0.800 3 2011 2017
dbSNP: rs8109288
rs8109288
2 19 16074749 non coding transcript exon variant G/A snp 3.5E-02 0.800 3 2011 2016
dbSNP: rs9399137
rs9399137
11 0.923 0.107 6 135097880 intron variant T/C snp 0.21 0.800 3 2009 2014
dbSNP: rs10761731
rs10761731
6 10 63267850 intron variant A/T snp 0.38 0.800 2 2011 2016
dbSNP: rs11082304
rs11082304
6 18 23141009 intron variant G/C,T snp 0.43 0.800 2 2011 2017
dbSNP: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2011 2017
dbSNP: rs3731211
rs3731211
5 9 21986848 intron variant T/A snp 0.74 0.800 2 2011 2017
dbSNP: rs3819299
rs3819299
3 1.000 6 31354590 non coding transcript exon variant T/G snp 7.7E-02 6.1E-02 0.800 2 2011 2017
dbSNP: rs4895441
rs4895441
10 0.923 0.071 6 135105435 intergenic variant A/G snp 0.23 0.800 2 2014 2016
dbSNP: rs505404
rs505404
2 11 243268 non coding transcript exon variant T/G snp 0.29 0.800 2 2011 2014
dbSNP: rs6065
rs6065
4 0.923 0.143 17 4933086 missense variant C/T snp 9.8E-02 0.12 0.800 2 2010 2011
dbSNP: rs6141
rs6141
3 1.000 0.071 3 184372478 3 prime UTR variant C/G,T snp 4.0E-06; 0.56 0.61 0.800 2 2010 2011
dbSNP: rs7342306
rs7342306
1 12 6181927 regulatory region variant G/A snp 0.35 0.800 2 2011 2016
dbSNP: rs7641175
rs7641175
4 3 18269920 intron variant G/A snp 0.81 0.800 2 2011 2017
dbSNP: rs1034566
rs1034566
1 22 19996754 intron variant C/G,T snp 0.24 0.800 1 2011 2011
dbSNP: rs10512472
rs10512472
1 17 35557785 missense variant T/C snp 0.21 0.19 0.800 1 2011 2011
dbSNP: rs10914144
rs10914144
3 1 171980610 intron variant T/C snp 0.77 0.800 1 2011 2011
dbSNP: rs11602954
rs11602954
2 11 202856 intron variant G/A snp 0.18 0.800 1 2014 2014
dbSNP: rs11628318
rs11628318
1 14 102573750 regulatory region variant T/A,C snp 0.64 0.800 1 2011 2011
dbSNP: rs11789898
rs11789898
1 9 134060541 intron variant G/T snp 0.14 0.800 1 2011 2011
dbSNP: rs13300663
rs13300663
4 9 4814948 intron variant G/A,C snp 0.20 0.800 1 2011 2011
dbSNP: rs1668871
rs1668871
3 1 205268009 intron variant T/C,G snp 0.31 0.800 1 2011 2011