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: rs1048943
rs1048943
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2009 2009
dbSNP: rs13181
rs13181
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 1.000 1 2013 2013
dbSNP: rs1442744764
rs1442744764
1 1.000 0.120 9 136496490 missense variant G/A snv 4.2E-06 0.010 1.000 1 2007 2007
dbSNP: rs145036301
rs145036301
5 0.851 0.120 19 11513899 missense variant A/G snv 2.7E-03 9.4E-04 0.010 1.000 1 2018 2018
dbSNP: rs1494555
rs1494555
8 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 0.010 1.000 1 2011 2011
dbSNP: rs17655
rs17655
52 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 0.010 1.000 1 2006 2006
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 2010 2010
dbSNP: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
dbSNP: rs1801195
rs1801195
WRN
8 0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 0.010 1.000 1 2013 2013
dbSNP: rs2069812
rs2069812
IL5
5 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2011 2011
dbSNP: rs2835931
rs2835931
4 1.000 0.120 21 37749345 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs3742330
rs3742330
24 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs477145
rs477145
4 1.000 0.120 21 31390097 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs61733010
rs61733010
2 0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 0.010 1.000 1 2007 2007
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2011 2011
dbSNP: rs745738344
rs745738344
TNF
28 0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs752317734
rs752317734
5 0.851 0.120 8 90020913 missense variant T/C snv 4.9E-06 0.010 1.000 1 2018 2018
dbSNP: rs753716491
rs753716491
2 1.000 0.120 9 77922196 missense variant T/A snv 0.010 1.000 1 2019 2019
dbSNP: rs753861648
rs753861648
2 1.000 0.120 19 54906742 missense variant G/C snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs758837678
rs758837678
2 0.925 0.120 8 90001503 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs854560
rs854560
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
dbSNP: rs938448224
rs938448224
7 0.807 0.160 17 42207711 missense variant T/G snv 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs9808753
rs9808753
17 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 0.010 1.000 1 2011 2011
dbSNP: rs9514828
rs9514828
12 0.752 0.440 13 108269025 intron variant C/T snv 0.35 0.020 1.000 2 2012 2012