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: rs1004819
rs1004819
IL23R ; C1orf141
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs1005753
rs1005753
PADI2
1 1.000 0.120 1 17118274 intron variant G/T snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs10174098
rs10174098
ITGAV
3 0.882 0.200 2 186628015 intron variant G/A snv 0.62 0.010 < 0.001 1 2014 2014
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.010 1.000 1 2018 2018
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs10263447
rs10263447
NPSR1 ; NPSR1-AS1
1 1.000 0.120 7 34820377 intron variant G/C snv 0.14 0.010 1.000 1 2010 2010
dbSNP: rs1035142
rs1035142
FLACC1
7 0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 0.010 1.000 1 2016 2016
dbSNP: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2009 2009
dbSNP: rs10461703
rs10461703
ADAMTS12
1 1.000 0.120 5 33596119 intron variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs10468473
rs10468473 		1 1.000 0.120 17 12224359 intergenic variant T/C snv 8.8E-02 0.010 1.000 1 2015 2015
dbSNP: rs104895218
rs104895218
TNFRSF1A
5 0.827 0.240 12 6334099 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs104895219
rs104895219
TNFRSF1A
5 0.827 0.240 12 6333823 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs104895221
rs104895221
TNFRSF1A
2 0.925 0.200 12 6333490 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs104895271
rs104895271
TNFRSF1A
6 0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 0.010 1.000 1 2013 2013
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 2008 2008
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 < 0.001 1 2012 2012
dbSNP: rs1055311
rs1055311
AIRE
1 1.000 0.120 21 44289685 synonymous variant C/G;T snv 2.0E-05; 0.23 0.010 1.000 1 2013 2013
dbSNP: rs1058587
rs1058587
GDF15
4 0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 0.010 1.000 1 2015 2015
dbSNP: rs1059702
rs1059702
IRAK1
7 0.807 0.280 X 154018741 missense variant A/G snv 0.72 0.010 1.000 1 2017 2017
dbSNP: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 < 0.001 1 2011 2011
dbSNP: rs1063539
rs1063539
ADIPOQ ; ADIPOQ-AS1
5 0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10 0.010 < 0.001 1 2020 2020
dbSNP: rs10754558
rs10754558
NLRP3
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs10840759
rs10840759
CLEC4A
3 0.882 0.200 12 8138610 intron variant C/T snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs10841845
rs10841845
CLEC4E
2 0.925 0.200 12 8533837 3 prime UTR variant A/G snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs10954213
rs10954213
IRF5
11 0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 0.010 1.000 1 2014 2014