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: rs548234
rs548234
ATG5
11 0.763 0.360 6 106120159 intron variant C/T snv 0.76 0.830 1.000 4 2009 2017
dbSNP: rs6445975
rs6445975
PXK
4 0.851 0.160 3 58384450 intron variant G/T snv 0.63 0.830 1.000 4 2008 2012
dbSNP: rs10239340
rs10239340
TNPO3
1 1.000 0.080 7 129028456 intron variant T/A;G snv 0.700 1.000 3 2008 2014
dbSNP: rs12531711
rs12531711
TNPO3
5 0.827 0.200 7 128977412 intron variant A/C;G snv 0.800 1.000 3 2011 2017
dbSNP: rs12720270
rs12720270
TYK2
4 0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 0.030 1.000 3 2009 2019
dbSNP: rs1385374
rs1385374
SLC15A4
1 1.000 0.080 12 128816149 intron variant C/T snv 9.1E-02 0.810 1.000 3 2009 2016
dbSNP: rs1800896
rs1800896
IL10 ; IL19
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2018 2019
dbSNP: rs187238
rs187238
IL18
48 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 0.333 3 2012 2015
dbSNP: rs1946518
rs1946518
IL18
46 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.667 3 2012 2015
dbSNP: rs2221903
rs2221903
IL21 ; IL21-AS1
12 0.752 0.360 4 122617757 intron variant C/T snv 0.77 0.030 1.000 3 2008 2015
dbSNP: rs2234693
rs2234693
ESR1
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.030 1.000 3 2011 2017
dbSNP: rs35000415
rs35000415
IRF5
1 1.000 0.080 7 128945562 intron variant C/T snv 9.0E-02 0.700 1.000 3 2015 2017
dbSNP: rs3757173
rs3757173
TNFAIP3 ; WAKMAR2
1 1.000 0.080 6 137869017 intron variant A/G snv 0.20 0.720 1.000 3 2012 2016
dbSNP: rs3821236
rs3821236
STAT4
3 0.882 0.160 2 191038032 intron variant G/A snv 0.25 0.810 1.000 3 2008 2016
dbSNP: rs57095329
rs57095329
MIR3142HG
25 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.030 1.000 3 2011 2016
dbSNP: rs573775
rs573775
ATG5
4 0.851 0.320 6 106316991 intron variant G/A snv 0.34 0.720 1.000 3 2008 2018
dbSNP: rs7601754
rs7601754
STAT4
3 0.882 0.160 2 191075725 intron variant G/A;T snv 0.810 1.000 3 2010 2013
dbSNP: rs7941765
rs7941765 		3 0.882 0.160 11 128629105 intron variant T/C snv 0.66 0.700 1.000 3 2015 2019
dbSNP: rs907715
rs907715
IL21
11 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.030 1.000 3 2008 2015
dbSNP: rs9462027
rs9462027
UHRF1BP1
1 1.000 0.080 6 34829464 intron variant G/A snv 0.37 0.700 1.000 3 2015 2017
dbSNP: rs9652601
rs9652601
CLEC16A
1 1.000 0.080 16 11080508 intron variant G/A snv 0.34 0.700 1.000 3 2015 2017
dbSNP: rs10048743
rs10048743
IKZF2
1 1.000 0.080 2 213025508 intron variant G/T snv 0.78 0.700 1.000 2 2015 2016
dbSNP: rs10181656
rs10181656
STAT4
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.020 1.000 2 2008 2010
dbSNP: rs10774625
rs10774625
ATXN2
13 0.763 0.320 12 111472415 intron variant A/G snv 0.66 0.700 1.000 2 2015 2016
dbSNP: rs10911363
rs10911363
NCF2 ; SMG7
2 0.925 0.120 1 183580622 intron variant G/T snv 0.30 0.710 1.000 2 2009 2011