Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 5
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs7759127
HLA-B ; HLA-C
0.925 0.040 6 31273211 intron variant T/G snv 0.11 5
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs1333955
PACRG
0.851 0.080 6 162792422 intron variant T/A;C snv 4
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 4
rs1040079
PACRG
0.882 0.040 6 162792995 intron variant A/G snv 0.31 3
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 3
rs3762318
C1orf141
0.925 0.040 1 67131436 intron variant G/A snv 0.83 3
rs12631031
PARL
0.925 0.040 3 183857982 intron variant G/A snv 0.12 2
rs2270368
SNX20
0.925 0.080 16 50680424 intron variant G/A;C snv 2
rs2275606
LOC101928661 ; ADGB
0.925 0.040 6 146597814 intron variant G/A snv 7.7E-02 2
rs7298930
LRRK2
0.925 0.040 12 40325698 intron variant A/C;G;T snv 2
rs7653061
MIR4448 ; PARL
0.925 0.040 3 183886132 intron variant T/G snv 0.12 2
rs8057341
NOD2
0.925 0.080 16 50704069 intron variant A/G snv 0.68 2
rs10414149
SIGLEC5
1.000 0.040 19 51624491 intron variant A/G snv 0.30 1
rs10507522
LOC107984576
1.000 0.040 13 43904864 intron variant A/G snv 0.11 1
rs10817758
DELEC1
1.000 0.040 9 115381654 intron variant C/T snv 0.13 1
rs11174812
SLC2A13
1.000 0.040 12 40031285 intron variant C/T snv 0.36 1