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: 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 0.700 1.000 1 2013 2013
dbSNP: rs79575701
rs79575701
ZBTB7C
3 0.882 0.120 18 48053250 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs79893749
rs79893749
CCR3
6 0.807 0.120 3 46212159 intron variant C/T snv 0.10 0.700 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: rs864089
rs864089
PRICKLE2
3 0.882 0.120 3 64258442 intron variant T/C snv 0.22 0.700 1.000 1 2017 2017
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: rs2284033
rs2284033
IL2RB
7 0.790 0.160 22 37137994 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs6894249
rs6894249
IRF1-AS1
9 0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs10174238
rs10174238
STAT4
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
9 0.776 0.200 22 21568615 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
ATXN2
15 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7775055
rs7775055 		7 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
IL2RA
8 0.776 0.240 10 6053447 intron variant A/T snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs6679677
rs6679677
PHTF1
26 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs34536443
rs34536443
TYK2
25 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013