Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6570989
GRIK2
1.000 0.080 6 101509537 intron variant G/A snv 0.25 1
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs16969868
FAM155A
1.000 0.080 13 107219364 intron variant G/C snv 3.8E-02 1
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 3
rs378042
STARD4-AS1 ; LOC105369177
1.000 0.080 5 111524099 intron variant G/A snv 1
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 8
rs1465781973
ANKK1
1.000 0.080 11 113395026 missense variant C/T snv 2.0E-05 1
rs777160724
ANKK1
1.000 0.080 11 113396169 missense variant A/G snv 4.0E-06 1
rs2734849
ANKK1
1.000 0.080 11 113399438 missense variant A/C;G snv 4.5E-06; 0.39 1
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6278
DRD2
1.000 0.080 11 113410002 3 prime UTR variant C/A snv 0.14 2
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1334465665
DRD2
1.000 0.080 11 113414400 missense variant C/T snv 2.1E-05 1
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs4274224
DRD2
1.000 0.080 11 113448730 intron variant G/A snv 0.49 1
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs4648317
DRD2
1.000 0.080 11 113460810 intron variant G/A snv 0.17 1
rs3758987
HTR3B
0.925 0.080 11 113904553 upstream gene variant T/C snv 0.32 4
rs4938056
HTR3B
0.925 0.080 11 113915817 intron variant C/T snv 0.51 2
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1486012 0.925 0.080 3 114120575 intergenic variant A/T snv 0.53 2
rs2399496
DRD3
0.925 0.080 3 114127166 downstream gene variant T/A snv 0.45 2
rs963468
DRD3
0.925 0.080 3 114144040 intron variant G/A snv 0.30 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57