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: rs564732150
rs564732150
MUC22
1 1.000 0.040 6 31028355 missense variant C/T snv 0.700 1.000 1 2010 2010
dbSNP: rs5754467
rs5754467
YDJC ; CCDC116
4 0.851 0.160 22 21630805 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs5844572
rs5844572
MIF ; MIF-AS1
11 0.752 0.360 22 23893562 intron variant -/ATTC delins 0.010 1.000 1 2019 2019
dbSNP: rs58721818
rs58721818 		4 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6073976
rs6073976 		1 1.000 0.040 20 45980011 upstream gene variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs624988
rs624988 		2 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs6726035
rs6726035 		3 0.882 0.120 2 204251279 regulatory region variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs6793295
rs6793295
LRRC34
6 0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 0.010 1.000 1 2016 2016
dbSNP: rs6832151
rs6832151 		2 0.925 0.160 4 40301616 intergenic variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs685985
rs685985 		1 1.000 0.040 8 60652405 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7190018
rs7190018
ITGAM
1 1.000 0.040 16 31290157 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs753727908
rs753727908
FCGR3A
1 1.000 0.040 1 161544759 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs755460305
rs755460305
KNG1
4 0.882 0.080 3 186732650 missense variant C/A snv 0.010 1.000 1 2002 2002
dbSNP: rs7601754
rs7601754
STAT4
3 0.882 0.160 2 191075725 intron variant G/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs77583790
rs77583790
IL12A-AS1
3 0.882 0.080 3 159976265 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs7774954
rs7774954
HLA-DQB2
2 0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs7900522
rs7900522
LRMDA
1 1.000 0.040 10 76350213 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7934606
rs7934606
MUC2
2 1.000 0.040 11 1100037 intron variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs8192284
rs8192284
IL6R
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs883770
rs883770
GSDMB
1 1.000 0.040 17 39907128 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9275245
rs9275245 		2 0.925 0.160 6 32693166 intergenic variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs960709
rs960709
TNIP1
5 0.882 0.120 5 151081488 intron variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs150840924
rs150840924
LMNA
7 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs774359492
rs774359492
WDHD1
7 0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012