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: rs9340799
rs9340799
62 0.583 0.680 6 151842246 intron variant A/G snv 0.32 0.010 < 0.001 1 2008 2008
dbSNP: rs884164
rs884164
2 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs872129
rs872129
2 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs7944926
rs7944926
7 0.807 0.200 11 71454579 intron variant A/G snv 0.54 0.010 1.000 1 2015 2015
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 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 2013 2013
dbSNP: rs753152
rs753152
6 0.882 0.160 17 42761487 intron variant T/G snv 0.12 0.010 < 0.001 1 2017 2017
dbSNP: rs752596535
rs752596535
14 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 0.010 1.000 1 2003 2003
dbSNP: rs751141
rs751141
16 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 0.010 1.000 1 2010 2010
dbSNP: rs750249283
rs750249283
2 0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs745738344
rs745738344
TNF
28 0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 0.010 < 0.001 1 2005 2005
dbSNP: rs738409
rs738409
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2017 2018
dbSNP: rs72653706
rs72653706
32 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 0.010 < 0.001 1 2011 2011
dbSNP: rs7043199
rs7043199
2 1.000 0.040 9 2621145 intron variant T/A snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs699947
rs699947
67 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs6993770
rs6993770
9 0.925 0.080 8 105569300 intron variant A/T snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 < 0.001 2 2001 2003
dbSNP: rs6921438
rs6921438
10 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs6834314
rs6834314
10 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 0.010 1.000 1 2017 2017
dbSNP: rs6749704
rs6749704
5 0.827 0.240 2 227813126 intron variant T/C snv 0.24 0.010 < 0.001 1 2016 2016
dbSNP: rs6742078
rs6742078
13 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2013 2013
dbSNP: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2004 2004
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2000 2000
dbSNP: rs5880
rs5880
10 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 0.010 1.000 1 2000 2000