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: rs2227945
rs2227945
2 1.000 0.080 17 43092113 missense variant T/C;G snv 2.5E-03 1.0E-02 0.010 1.000 1 2000 2000
dbSNP: rs3218674
rs3218674
ATM
2 1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 0.010 1.000 1 2002 2002
dbSNP: rs1805087
rs1805087
MTR
135 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2003 2003
dbSNP: rs1799725
rs1799725
1 6 159692840 missense variant A/G snv 0.010 1.000 1 2006 2006
dbSNP: rs4880
rs4880
131 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2006 2006
dbSNP: rs764643047
rs764643047
5 0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs149627368
rs149627368
REL
1 2 60922344 missense variant T/C snv 1.5E-04 1.0E-04 0.010 1.000 1 2007 2007
dbSNP: rs1799782
rs1799782
151 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs25487
rs25487
205 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 < 0.001 1 2009 2009
dbSNP: rs12144309
rs12144309
1 1 113772871 intron variant C/T snv 0.19 0.010 1.000 1 2010 2010
dbSNP: rs12566340
rs12566340
3 0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs3789607
rs3789607
1 1 113823812 intron variant T/C snv 0.21 0.010 1.000 1 2010 2010
dbSNP: rs3811021
rs3811021
2 1.000 0.080 1 113814041 3 prime UTR variant A/G snv 0.15 0.010 1.000 1 2010 2010
dbSNP: rs1053023
rs1053023
4 0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 0.010 1.000 1 2011 2011
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: 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: 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: rs1800477
rs1800477
12 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2012 2012
dbSNP: rs6857600
rs6857600
3 0.925 0.120 4 88144923 intron variant C/T snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs9610
rs9610
4 0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 0.010 1.000 1 2012 2012
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2012 2013
dbSNP: rs141185042
rs141185042
1 12 32707409 missense variant A/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2013 2013
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: rs2509049
rs2509049
6 0.827 0.160 11 119095811 upstream gene variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs355689
rs355689
2 1.000 0.040 4 77586643 intron variant T/A;C snv 0.010 1.000 1 2013 2013