Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs2044117
NALCN ; NALCN-AS1
13 101055958 intron variant G/A snv 0.19 2
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs1341402
DAOA-AS1
1.000 0.040 13 105463160 intron variant T/C snv 0.16 2
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs778294
DAOA ; DAOA-AS1
0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
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
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4