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: rs1000113
rs1000113
IRGM
2 0.925 0.040 5 150860514 intron variant C/T snv 0.13 0.010 1.000 1 2009 2009
dbSNP: rs10035653
rs10035653
EXOC3 ; EXOC3-AS1
1 1.000 0.040 5 442675 non coding transcript exon variant G/A;T snv 9.1E-02; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs10063949
rs10063949
SLC23A1
4 0.882 0.080 5 139383837 intron variant T/C snv 0.48 0.010 1.000 1 2014 2014
dbSNP: rs10114470
rs10114470
TNFSF15
4 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs10174238
rs10174238
STAT4
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.010 1.000 1 2010 2010
dbSNP: rs1020856343
rs1020856343
SLC22A5
5 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs10226620
rs10226620
MAFK ; TMEM184A
4 1.000 0.040 7 1541881 3 prime UTR variant T/C snv 0.69 0.010 < 0.001 1 2017 2017
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2010 2010
dbSNP: rs10415946
rs10415946
CEACAM6
1 1.000 0.040 19 41755151 intron variant A/G snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs10416839
rs10416839 		1 1.000 0.040 19 41776424 intron variant G/T snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
11 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 0.010 1.000 1 2012 2012
dbSNP: rs1048230
rs1048230
SLC11A2
5 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2000 2000
dbSNP: rs104895467
rs104895467
NOD2
5 0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04 0.010 < 0.001 1 2018 2018
dbSNP: rs104895486
rs104895486
NOD2
2 0.925 0.040 16 50716670 missense variant C/G;T snv 4.0E-06; 8.0E-05 0.010 1.000 1 2006 2006
dbSNP: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2010 2010
dbSNP: rs1049793
rs1049793
AOC1 ; LOC105375567
4 0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37 0.010 1.000 1 2006 2006
dbSNP: rs10499563
rs10499563
STEAP1B
7 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
10 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2010 2010
dbSNP: rs1052571
rs1052571
CASP9
4 0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 0.010 1.000 1 2011 2011
dbSNP: rs1088967
rs1088967 		4 0.851 0.080 X 127010099 intergenic variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs10925019
rs10925019
NLRP3
2 0.925 0.040 1 247432548 intron variant C/T snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs10951982
rs10951982
RAC1
5 0.851 0.160 7 6382925 intron variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs11264799
rs11264799
FCRL3
6 0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 0.010 1.000 1 2007 2007
dbSNP: rs1127233
rs1127233
MUC13
2 0.925 0.040 3 124908177 missense variant T/G snv 0.24 0.26 0.010 1.000 1 2006 2006
dbSNP: rs1128535
rs1128535
TRAIP
2 0.925 0.040 3 49828959 3 prime UTR variant C/A;T snv 0.48 0.010 1.000 1 2008 2008