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: rs7127214
rs7127214
PRR5L
6 0.807 0.120 11 36322143 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs72698115
rs72698115
IL6R ; IL6R-AS1
6 0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
JAZF1
6 0.807 0.120 7 28147725 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
6 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 0.800 1.000 1 2013 2013
dbSNP: rs79893749
rs79893749
CCR3
6 0.807 0.120 3 46212159 intron variant C/T snv 0.10 0.800 1.000 1 2013 2013
dbSNP: rs8129030
rs8129030
RUNX1
7 0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 0.700 1.000 1 2013 2013
dbSNP: rs9532434
rs9532434
COG6
8 0.807 0.120 13 39781776 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11893432
rs11893432
STAT4
5 0.827 0.120 2 191057148 intron variant C/G snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs12434551
rs12434551 		1 1.000 0.120 14 68786647 downstream gene variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4705862
rs4705862
IRF1-AS1
1 1.000 0.120 5 132477527 intron variant A/T snv 0.51 0.700 1.000 1 2013 2013