Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs143396368
FXN
0.807 0.200 9 69072623 missense variant G/A;C snv 3.2E-05; 8.0E-06 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6