Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs2072621
GPR50-AS1 ; GPR50
0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs10838524
CRY2
0.851 0.120 11 45848626 intron variant A/G snv 0.42 5
rs11541353
NPAS2-AS1 ; NPAS2
0.851 0.120 2 100977729 missense variant C/T snv 0.14 0.14 4
rs2314339
NR1D1
0.851 0.120 17 40096959 intron variant C/T snv 0.20 4
rs2028122
RORA ; RORA-AS1
0.851 0.120 15 60549076 intron variant A/G snv 0.51 4
rs7019241
GOLM1
1.000 0.040 9 86078545 intron variant C/G;T snv 1
rs731779
HTR2A
1.000 0.040 13 46877903 intron variant A/C snv 0.16 1
rs1079610
LOC105378409 ; OPN4
1.000 0.040 10 86662359 missense variant C/T snv 0.70 0.70 1
rs2675703
OPN4
1.000 0.040 10 86654812 missense variant C/T snv 0.10 0.10 1