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: rs10129516
rs10129516
1 1.000 0.040 14 63133372 intron variant T/A;C snv 0.710 < 0.001 1 2017 2017
dbSNP: rs1056836
rs1056836
58 0.581 0.680 2 38071060 missense variant G/C snv 0.51 0.010 < 0.001 1 2007 2007
dbSNP: rs1202989817
rs1202989817
18 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs1256049
rs1256049
32 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 0.010 < 0.001 1 2014 2014
dbSNP: rs1457582183
rs1457582183
5 0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs17387019
rs17387019
1 1.000 0.040 12 25111325 intron variant G/A snv 5.7E-02 0.010 < 0.001 1 2012 2012
dbSNP: rs1800907
rs1800907
3 0.925 0.120 7 142800425 upstream gene variant T/C snv 0.56 0.010 < 0.001 1 2011 2011
dbSNP: rs2010963
rs2010963
82 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 < 0.001 1 2013 2013
dbSNP: rs2020917
rs2020917
4 0.851 0.160 22 19941361 intron variant C/T snv 0.22 0.010 < 0.001 1 2019 2019
dbSNP: rs368163858
rs368163858
1 1.000 0.040 19 1627376 missense variant C/T snv 2.5E-05 2.1E-05 0.010 < 0.001 1 2012 2012
dbSNP: rs372201428
rs372201428
3 0.882 0.120 17 7676181 missense variant G/A;C snv 1.2E-05 0.010 < 0.001 1 2013 2013
dbSNP: rs3756712
rs3756712
10 0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs3918242
rs3918242
54 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 < 0.001 1 2018 2018
dbSNP: rs4880
rs4880
131 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 < 0.001 1 2013 2013
dbSNP: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 < 0.001 1 2012 2012
dbSNP: rs700518
rs700518
13 0.732 0.320 15 51236915 synonymous variant T/C snv 0.43 0.40 0.010 < 0.001 1 2007 2007
dbSNP: rs75391579
rs75391579
5 0.827 0.280 9 34648170 missense variant A/G snv 1.4E-03 1.9E-03 0.010 < 0.001 1 2006 2006
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 < 0.001 1 2012 2012
dbSNP: rs763000109
rs763000109
TNF
9 0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 0.010 < 0.001 1 2013 2013
dbSNP: rs777161444
rs777161444
1 1.000 0.040 1 150817123 missense variant C/T snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2015 2015
dbSNP: rs833061
rs833061
42 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs1799969
rs1799969
38 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.040 0.500 4 2003 2016
dbSNP: rs11556218
rs11556218
27 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.020 0.500 2 2010 2018
dbSNP: rs11674184
rs11674184
1 1.000 0.040 2 11581409 intron variant T/A;G snv 0.710 0.500 2 2017 2019
dbSNP: rs17576
rs17576
73 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.020 0.500 2 2009 2016