Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 4
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs3135499
NOD2
0.882 0.160 16 50732216 splice donor variant A/C snv 0.45 3
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs4790522
TRPV1
0.925 0.080 17 3566559 3 prime UTR variant A/C snv 0.55 2
rs56267605 1.000 0.080 4 122441954 intergenic variant A/C snv 0.29 2
rs7183955
RORA
0.925 0.080 15 60757370 intron variant A/C snv 0.24 2
rs1012307
LINC01931 ; MMADHC-DT
1.000 0.080 2 149798707 intron variant A/C snv 4.9E-02 1
rs11048311 1.000 0.080 12 25869205 downstream gene variant A/C snv 0.18 1
rs11635191
CCDC33
1.000 0.080 15 74257709 intron variant A/C snv 0.62 1
rs1538084 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 1
rs229283
ALG9
1.000 0.080 11 111826373 intron variant A/C snv 1
rs2540493
LTA4H
1.000 0.080 12 96022064 intron variant A/C snv 0.17 1
rs3087271 1.000 0.080 2 113137623 downstream gene variant A/C snv 0.22 1
rs3136598
TNFSF10
1.000 0.080 3 172508962 intron variant A/C snv 0.70 1
rs4673659
ERBB4
1.000 0.080 2 212325005 intron variant A/C snv 0.69 1
rs7010969
MSC-AS1 ; TRPA1
1.000 0.080 8 72070130 intron variant A/C snv 0.69 1
rs7086533
LINC02660
1.000 0.080 10 3926521 intron variant A/C snv 0.91 1
rs7219080
GSDMA
1.000 0.080 17 39958263 intron variant A/C snv 0.65 1
rs7305461 1.000 0.080 12 56056091 intergenic variant A/C snv 0.49 1
rs73132886
AP3B1
1.000 0.080 5 78052816 intron variant A/C snv 2.6E-02 1
rs7551641 1.000 0.080 1 119475304 downstream gene variant A/C snv 6.6E-02 1
rs78930606 1.000 0.080 6 118757489 upstream gene variant A/C snv 1.7E-02 1