Source: ALL
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: 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 2019 2019
dbSNP: rs1800630
rs1800630
17 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 0.010 1.000 1 2019 2019
dbSNP: rs1801131
rs1801131
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
dbSNP: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.010 1.000 1 2019 2019
dbSNP: rs197388
rs197388
2 0.925 0.040 1 111754860 non coding transcript exon variant A/T snv 0.27 0.010 1.000 1 2018 2018
dbSNP: rs199746824
rs199746824
6 0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2001 2001
dbSNP: rs199752860
rs199752860
2 0.925 0.040 1 171652578 missense variant C/G snv 6.9E-04 1.5E-04 0.010 1.000 1 2000 2000
dbSNP: rs200208925
rs200208925
2 0.925 0.040 1 171652454 missense variant A/G snv 6.4E-05 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs200547613
rs200547613
2 0.925 0.040 1 171638675 missense variant C/T snv 4.8E-05 1.4E-05 0.010 1.000 1 2013 2013
dbSNP: rs200710076
rs200710076
2 0.925 0.040 10 13109198 missense variant C/A;G;T snv 8.0E-06; 2.0E-05; 2.4E-05 0.010 1.000 1 2004 2004
dbSNP: rs2149356
rs2149356
14 0.742 0.360 9 117711921 intron variant T/G snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs2157719
rs2157719
17 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 0.010 1.000 1 2012 2012
dbSNP: rs2234926
rs2234926
3 0.882 0.040 1 171652385 missense variant C/T snv 0.15 0.11 0.010 1.000 1 2008 2008
dbSNP: rs2234927
rs2234927
4 0.851 0.040 1 171638703 missense variant G/A;C snv 4.0E-06; 7.6E-04 0.010 1.000 1 2000 2000
dbSNP: rs2567206
rs2567206
7 0.827 0.200 2 38076389 non coding transcript exon variant G/A snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs267606929
rs267606929
5 0.827 0.120 10 13132098 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs267607161
rs267607161
TTR
16 0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs284489
rs284489
3 0.882 0.080 8 104945792 intron variant A/G snv 0.45 0.010 1.000 1 2012 2012
dbSNP: rs28936700
rs28936700
9 0.776 0.120 2 38075207 missense variant C/G;T snv 5.0E-06; 3.2E-04 0.010 1.000 1 2016 2016
dbSNP: rs35703638
rs35703638
1 1.000 0.040 5 111106140 missense variant G/A snv 8.3E-03 4.1E-03 0.010 1.000 1 2005 2005
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs369115487
rs369115487
1 1.000 0.040 2 38075373 missense variant T/C snv 1.6E-05 1.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs372487178
rs372487178
2 0.925 0.040 11 62616748 missense variant C/T snv 2.1E-05 0.010 1.000 1 2015 2015
dbSNP: rs3766355
rs3766355
3 0.882 0.040 1 78491756 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs3858145
rs3858145
3 0.882 0.040 10 68252081 regulatory region variant A/G snv 0.33 0.010 1.000 1 2012 2012