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: rs1800925
rs1800925
IL13 ; TH2LCRR
37 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.030 1.000 3 2009 2011
dbSNP: rs2066845
rs2066845
NOD2
46 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.030 1.000 3 2004 2010
dbSNP: rs4112788
rs4112788 		4 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 0.030 0.667 3 2010 2014
dbSNP: rs7530511
rs7530511
IL23R ; C1orf141
12 0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 0.030 1.000 3 2008 2012
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.020 1.000 2 2006 2014
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
14 0.716 0.440 1 67228519 intron variant A/G;T snv 0.020 1.000 2 2012 2014
dbSNP: rs114212579
rs114212579
CYP21A2 ; SKIV2L
1 1.000 0.080 6 31968280 non coding transcript exon variant G/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114265779
rs114265779
TRIM26
1 1.000 0.080 6 30213844 upstream gene variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114383947
rs114383947
MUC22
1 1.000 0.080 6 31010940 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114598684
rs114598684
MICA
1 1.000 0.080 6 31413173 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114757170
rs114757170
PPP1R10 ; MRPS18B
1 1.000 0.080 6 30618254 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115112280
rs115112280
HCG23 ; TSBP1-AS1
1 1.000 0.080 6 32390772 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs115145466
rs115145466 		1 1.000 0.080 6 32251264 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115429782
rs115429782
HLA-B ; LINC02571 ; LOC112267902
1 1.000 0.080 6 31297975 intron variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs115429849
rs115429849
MICC
1 1.000 0.080 6 30416827 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115529844
rs115529844
LOC105375010
1 1.000 0.080 6 29850244 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs115618145
rs115618145
TRIM31
1 1.000 0.080 6 30102498 upstream gene variant C/G snv 0.700 1.000 1 2019 2019
dbSNP: rs115645848
rs115645848
GABBR1
1 1.000 0.080 6 29622938 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115872194
rs115872194
BAG6
1 1.000 0.080 6 31639897 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115928623
rs115928623
HLA-A ; MICD
1 1.000 0.080 6 29971371 intron variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116199901
rs116199901
HCG18 ; HCG17
1 1.000 0.080 6 30315875 intron variant G/C snv 0.700 1.000 1 2019 2019
dbSNP: rs116340302
rs116340302
MCCD1 ; RPL15P4
1 1.000 0.080 6 31528604 non coding transcript exon variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116805908
rs116805908
POU5F1 ; PSORS1C3
1 1.000 0.080 6 31173746 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs12044149
rs12044149
C1orf141
2 0.925 0.080 1 67135003 intron variant G/C;T snv 0.710 1.000 1 2015 2015
dbSNP: rs12188300
rs12188300 		6 0.807 0.120 5 159402519 intron variant A/G;T snv 0.800 1.000 1 2010 2010