Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs2377339
NCK2
2 105840835 intron variant A/G snv 4.8E-02 2
rs764987358
ANGPT1
1.000 0.160 8 107347040 missense variant C/A snv 8.0E-06 1.4E-05 2
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs7118900
ANKK1
11 113396099 missense variant G/A snv 0.25 0.25 1
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
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs1075650
IER5L
9 129176634 3 prime UTR variant T/C snv 0.25 1
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs2073837
DBH-AS1 ; DBH
9 133657806 intron variant G/A snv 0.31 1
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8