Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs7628626
TIMMDC1 ; CD80
0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2
rs738792
MMP11
0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs11099592
HPSE
0.851 0.160 4 83309466 missense variant T/C snv 0.78 0.80 5
rs14304
CCL18
1.000 0.080 17 36071135 3 prime UTR variant T/C snv 0.78 2
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs10754339
VTCN1
0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs7186053
CDH1
1.000 0.080 16 68805390 intron variant A/G snv 0.69 1
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 2
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs2236142
HSCB ; CHEK2
0.827 0.120 22 28741956 5 prime UTR variant G/C snv 0.66 6
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs184432
TFF1
0.882 0.120 21 42367453 upstream gene variant G/A snv 0.64 3
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs225359
TFF1
0.882 0.120 21 42367327 upstream gene variant G/A snv 0.62 3
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs1360485
HMGB1
0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs8105637
TINCR
0.925 0.120 19 5566221 intron variant A/G snv 0.56 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62