Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1469698992
NUP214
0.776 0.080 9 131190453 missense variant G/A snv 8
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs1805502
GRIN2B
0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs7224199
SLC6A4
0.827 0.160 17 30196708 3 prime UTR variant G/T snv 0.49 7