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: rs121913459
rs121913459
25 0.672 0.160 9 130872896 missense variant C/T snv 0.020 1.000 2 2009 2019
dbSNP: rs1057519721
rs1057519721
4 0.882 0.120 9 5078360 missense variant A/G snv 0.010 1.000 1 2012 2012
dbSNP: rs1057519723
rs1057519723
2 0.925 0.120 9 5078362 missense variant A/C;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1057519743
rs1057519743
6 0.827 0.120 Y 1196852 missense variant A/C snv 0.010 1.000 1 2017 2017
dbSNP: rs11980379
rs11980379
3 0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 0.010 1.000 1 2017 2017
dbSNP: rs121434592
rs121434592
54 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs12430881
rs12430881
1 1.000 0.120 13 28020665 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs13107325
rs13107325
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.010 1.000 1 2018 2018
dbSNP: rs1346944271
rs1346944271
1 1.000 0.120 9 5090497 missense variant G/A snv 1.4E-05 0.010 1.000 1 2017 2017
dbSNP: rs156697
rs156697
25 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 0.010 < 0.001 1 2015 2015
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
dbSNP: rs189434316
rs189434316
2 0.925 0.120 14 92231568 intergenic variant A/T snv 4.1E-02 0.010 1.000 1 2017 2017
dbSNP: rs2393732
rs2393732
2 0.925 0.120 10 62007470 intron variant G/A snv 0.15 0.010 < 0.001 1 2019 2019
dbSNP: rs35958982
rs35958982
1 1.000 0.120 13 28034336 missense variant C/T snv 1.3E-02 5.0E-02 0.010 1.000 1 2019 2019
dbSNP: rs3780135
rs3780135
1 1.000 0.120 9 36840626 missense variant G/A snv 0.88 0.77 0.010 1.000 1 2019 2019
dbSNP: rs4925
rs4925
28 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 0.010 < 0.001 1 2015 2015
dbSNP: rs4948488
rs4948488
2 0.925 0.120 10 61925395 intron variant C/A;T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs4958351
rs4958351
3 0.882 0.120 5 153790814 intron variant G/A;T snv 0.31 0.010 < 0.001 1 2015 2015
dbSNP: rs529311209
rs529311209
2 0.925 0.120 22 40409754 missense variant G/A;C;T snv 3.3E-05; 8.2E-06 0.010 1.000 1 2012 2012
dbSNP: rs62527607
rs62527607
5 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs77375493
rs77375493
187 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2012 2012
dbSNP: rs780634396
rs780634396
5 0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs866838052
rs866838052
6 0.851 0.160 7 143267618 missense variant C/A snv 0.010 < 0.001 1 2015 2015