Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs202085145
SUOX
1.000 0.080 12 56002720 missense variant G/T snv 1.0E-03 5.6E-04 6
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs3761422
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
1.000 0.040 22 24430704 intron variant T/C snv 0.62 4
rs4822492
ADORA2A-AS1
1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs1132358
BAIAP3
1.000 0.040 16 1347814 synonymous variant C/T snv 0.44 0.39 3
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs2235632
BAIAP3
1.000 0.040 16 1343019 splice region variant G/A snv 0.46 0.42 3
rs3812047
GDNF-AS1 ; GDNF
1.000 0.040 5 37835296 intron variant C/G;T snv 3
rs4245146
DRD2
1.000 0.040 11 113447251 intron variant T/C snv 0.49 3
rs11030107
BDNF ; BDNF-AS
1.000 0.040 11 27673288 intron variant A/G snv 0.19 2
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2
rs1277240795
OGA
1.000 0.040 10 101791382 missense variant G/C snv 7.0E-06 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
rs2463107 1.000 0.040 12 79699537 intron variant A/C snv 0.36 2
rs2572431 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 2
rs2941026
CCKBR
1.000 0.040 11 6261042 intron variant A/G snv 0.51 2
rs2973050
GDNF-AS1 ; GDNF
1.000 0.040 5 37817242 intron variant A/G;T snv 2
rs34548976 1.000 0.040 7 31032854 intergenic variant C/T snv 0.39 2
rs3930965
AKR1C1
1.000 0.040 10 4971951 intron variant G/A;C snv 2
rs4813627 1.000 0.040 20 3074867 downstream gene variant A/G snv 0.51 2
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs61910731
COMT ; MIR4761
1.000 0.040 22 19963574 missense variant G/A;C;T snv 2.4E-05; 4.0E-06 2