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: rs968567
rs968567
FADS1 ; FADS2
7 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.810 1.000 4 2009 2019
dbSNP: rs10181656
rs10181656
STAT4
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.820 1.000 3 2012 2017
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
5 0.827 0.240 1 67222666 intron variant T/C snv 0.48 0.030 1.000 3 2012 2020
dbSNP: rs10774624
rs10774624
LINC02356
6 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.810 1.000 3 2014 2019
dbSNP: rs10903323
rs10903323
MSRA
8 0.807 0.160 8 10292057 intron variant A/G snv 0.15 0.030 1.000 3 2010 2013
dbSNP: rs11568821
rs11568821
PDCD1 ; LOC105373977
10 0.827 0.200 2 241851760 intron variant C/G;T snv 0.030 1.000 3 2007 2018
dbSNP: rs13031237
rs13031237
REL
3 1.000 0.120 2 60908994 intron variant G/T snv 0.25 0.810 1.000 3 2009 2012
dbSNP: rs13277113
rs13277113
BLK
18 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.030 1.000 3 2011 2017
dbSNP: rs13315591
rs13315591
FAM107A ; LOC107984079
4 0.925 0.160 3 58571114 intron variant T/C snv 0.15 0.800 1.000 3 2010 2012
dbSNP: rs17264332
rs17264332 		2 0.925 0.200 6 137684378 intron variant A/G;T snv 0.800 1.000 3 2014 2019
dbSNP: rs187238
rs187238
IL18
48 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 0.333 3 2005 2014
dbSNP: rs1946518
rs1946518
IL18
46 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.333 3 2005 2014
dbSNP: rs1953126
rs1953126
PHF19
3 1.000 0.120 9 120878222 intron variant T/C snv 0.68 0.710 1.000 3 2007 2009
dbSNP: rs1980493
rs1980493
BTNL2 ; TSBP1-AS1
10 0.776 0.400 6 32395438 intron variant T/C snv 0.13 0.700 1.000 3 2007 2011
dbSNP: rs204991
rs204991
GPSM3
3 0.882 0.200 6 32193589 intron variant T/C snv 0.21 0.710 1.000 3 2007 2016
dbSNP: rs206015
rs206015
NOTCH4
2 0.925 0.200 6 32214982 intron variant G/A snv 0.15 0.700 1.000 3 2007 2011
dbSNP: rs2071295
rs2071295
TNXB
2 0.925 0.120 6 32070923 intron variant C/T snv 0.25 0.700 1.000 3 2007 2011
dbSNP: rs2074488
rs2074488
HLA-B ; HLA-C
3 0.925 0.160 6 31272654 intron variant G/T snv 0.13 0.700 1.000 3 2007 2011
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 3 2007 2011
dbSNP: rs2239689
rs2239689
TNXB
2 0.925 0.120 6 32062507 intron variant G/A snv 0.33 0.25 0.700 1.000 3 2007 2011
dbSNP: rs2239804
rs2239804
HLA-DRA
5 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 0.700 1.000 3 2007 2011
dbSNP: rs2260000
rs2260000
PRRC2A
7 0.851 0.200 6 31625699 intron variant A/G snv 0.29 0.700 1.000 3 2007 2011
dbSNP: rs2277438
rs2277438
TNFSF11
5 0.827 0.160 13 42581032 intron variant G/A;C snv 0.030 0.333 3 2010 2019
dbSNP: rs2281829
rs2281829
UQCC2
1 1.000 0.120 6 33707865 intron variant A/G snv 0.40 0.700 1.000 3 2007 2011
dbSNP: rs2301888
rs2301888
PADI4
1 1.000 0.120 1 17346235 intron variant G/A snv 0.31 0.800 1.000 3 2014 2019