Disease: Obsessive-Compulsive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs301430
SLC1A1 ; SPATA6L
0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs2857766
MOG
0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 4
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs1477437491
NOS1AP
0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05 2