Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10052999
C6
1.000 0.080 5 41165642 intron variant C/T snv 7.5E-02 1
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs1010273
PRDM1 ; ATG5
0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02 3
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1012335
IFNAR1
0.925 0.080 21 33341701 intron variant G/C;T snv 2
rs1014509103
ADAMTS4
1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05 2
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 4
rs1040441824
PTS
0.882 0.200 11 112233502 missense variant A/G snv 2.1E-05 4
rs1042489
BIRC5
0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1046282
ERCC1 ; CD3EAP ; PPP1R13L
0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs10485505
ITCH
1.000 0.080 20 34437762 intron variant C/G;T snv 3