Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3930965
AKR1C1
1.000 0.040 10 4971951 intron variant G/A;C snv 2
rs11030107
BDNF ; BDNF-AS
1.000 0.040 11 27673288 intron variant A/G snv 0.19 2
rs2941026
CCKBR
1.000 0.040 11 6261042 intron variant A/G snv 0.51 2
rs61910731
COMT ; MIR4761
1.000 0.040 22 19963574 missense variant G/A;C;T snv 2.4E-05; 4.0E-06 2
rs8192506
DBI
1.000 0.040 2 119372265 missense variant A/C;G snv 4.0E-06; 2.5E-02 2
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2
rs2973050
GDNF-AS1 ; GDNF
1.000 0.040 5 37817242 intron variant A/G;T snv 2
rs1709393
LINC02085
1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs1960264
LOC105373148 ; SAT1
1.000 0.040 X 23781758 intron variant C/G;T snv 2
rs6470292
LOC105375743 ; LINC00964
1.000 0.040 8 124855801 intron variant A/G snv 0.17 2
rs683250
LOC107984425 ; DLG2
1.000 0.040 11 83565125 intron variant A/G;T snv 2
rs1277240795
OGA
1.000 0.040 10 101791382 missense variant G/C snv 7.0E-06 2
rs757281
RAPGEF3
1.000 0.040 12 47748635 non coding transcript exon variant C/A;G;T snv 2
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs1132358
BAIAP3
1.000 0.040 16 1347814 synonymous variant C/T snv 0.44 0.39 3
rs2235632
BAIAP3
1.000 0.040 16 1343019 splice region variant G/A snv 0.46 0.42 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs2111902
DAO
0.925 0.080 12 108884971 intron variant T/A;G snv 0.40 3
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs4623951
DAO
0.925 0.080 12 108878275 intron variant C/G;T snv 3
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs4245146
DRD2
1.000 0.040 11 113447251 intron variant T/C snv 0.49 3
rs1276624859
EIF4EBP1
0.925 0.080 8 38057134 missense variant G/A snv 3
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3