Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2281089
IL2RB
0.851 0.200 22 37136132 intron variant A/G snv 0.17 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
rs79589812
SPATC1L
0.882 0.080 21 46181088 intron variant T/A;C snv 4
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31