Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
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
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs1076562
DRD2
0.925 0.120 11 113425286 intron variant A/G snv 0.65 2
rs11214607
DRD2
1.000 0.040 11 113441417 intron variant T/G snv 0.16 2
rs2734839
DRD2
1.000 0.040 11 113415768 intron variant C/A;T snv 2
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs6278
DRD2
1.000 0.080 11 113410002 3 prime UTR variant C/A snv 0.14 2
rs767413934
DRD2
0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 2
rs104894220
DRD2
1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05 1
rs1079596
DRD2
11 113425897 intron variant C/A;T snv 1
rs1079727
DRD2
1.000 0.040 11 113418460 intron variant T/C snv 0.16 1
rs1110977
DRD2
1.000 0.040 11 113412643 missense variant T/A;C snv 7.0E-06 1
rs1116313
DRD2
1.000 0.080 11 113425385 intron variant A/G snv 0.45 1