DisGeNET - a database of gene-disease associations

Obsessive-Compulsive Disorder, C0028768

Variant: rs3780412 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs3780412

SLC1A1 ; SPATA6L

0.020

GeneticVariation

BEFREE

The A-A-G (rs301434-rs3780412-rs301443) haplotype was twice as common in OCD as in controls (P = 0.02).

30661718

2019

dbSNP:

rs3780412

SLC1A1 ; SPATA6L

0.020

GeneticVariation

BEFREE

Single-marker associations with OCD in the region (rs3780412 and rs2228622) demonstrated modest significance (permuted P = 0.045).

17894418

2007