Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738792
MMP11
0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs28382575
MMP11
0.851 0.120 22 23783502 synonymous variant T/C snv 2.2E-02 1.8E-02 5
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs757163626
MIR4761 ; COMT
0.827 0.120 22 19962726 missense variant C/T snv 1.6E-05 7.0E-06 5
rs139293
APOBEC3H
0.882 0.080 22 39100331 missense variant G/A;T snv 2.3E-04; 0.27 4
rs2281089
IL2RB
0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs540635787
CHEK2
0.851 0.200 22 28694073 missense variant G/A;C;T snv 1.7E-05 4
rs11090910
MIRLET7A3 ; MIRLET7BHG ; MIR4763 ; MIRLET7B
0.882 0.080 22 46111790 non coding transcript exon variant T/C snv 0.30 3
rs11703832
MIRLET7BHG
0.882 0.080 22 46108287 intron variant C/T snv 0.19 3
rs12170325
MIRLET7BHG
0.882 0.080 22 46106990 intron variant C/T snv 0.18 3
rs13053856
MIRLET7BHG
0.882 0.080 22 46104002 intron variant G/A;T snv 3
rs2236141
CHEK2 ; HSCB
0.882 0.080 22 28741882 5 prime UTR variant C/T snv 0.10 3
rs2267029
MMP11
0.882 0.080 22 23775729 intron variant A/G snv 0.92 3
rs5756523 0.882 0.080 22 37117508 intergenic variant T/A;C snv 3
rs663048
SEZ6L
0.882 0.080 22 26299111 missense variant G/A;T snv 4.2E-06; 0.19 3
rs745794582
CYP2D6 ; NDUFA6-DT ; LOC112268294
0.882 0.080 22 42130751 missense variant G/A snv 4.5E-06 3
rs746764639
MIR4761 ; COMT
0.882 0.080 22 19962714 missense variant T/C snv 2.4E-05 3.5E-05 3
rs750269833
CYP2D6 ; NDUFA6-DT ; LOC112268294
0.882 0.080 22 42129119 missense variant C/T snv 4.1E-06 3
rs876659871
CHEK2
0.882 0.080 22 28719462 missense variant C/T snv 7.0E-06 3
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs234709
CBS
0.827 0.200 21 43066854 intron variant C/T snv 7
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs4920037
CBS
0.851 0.080 21 43061781 intron variant G/A snv 4