DisGeNET - a database of gene-disease associations

Behcet Syndrome, C0004943

Variant: rs6318 ×

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:

rs6318

rs6318

HTR2C ; LOC105373313

0.010

GeneticVariation

BEFREE

The functional rs6318 G (Cys) allele was more frequent in BD patients than in controls (P=0.0036).Thus, 5HTR2C may have a role in BD.

2010