Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1465107
MAOA
1.000 0.040 X 43678769 intron variant A/G snv 1
rs2072743
MAOA
1.000 0.040 X 43740274 intron variant T/C snv 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs766020740
MIR4761 ; COMT
0.851 0.120 22 19963644 missense variant C/A snv 4.0E-06 5
rs1058172
CYP2D6 ; NDUFA6-DT
0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 4
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs140504
LOC107985554 ; BCR
0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs2075984
TPTEP2-CSNK1E ; CSNK1E
0.882 0.040 22 38294883 intron variant C/A;G;T snv 3
rs4468
BRD1
1.000 0.040 22 49774004 3 prime UTR variant T/C snv 0.53 2
rs6928
MAPK1
0.925 0.080 22 21760715 3 prime UTR variant C/G snv 0.49 2
rs13515
MAPK1
1.000 0.040 22 21761597 3 prime UTR variant C/T snv 0.16 1
rs140395831
LOC105373062 ; ARHGAP8 ; PRR5-ARHGAP8
1.000 0.040 22 44859739 missense variant A/C;G snv 3.3E-04; 4.0E-06 1