DisGeNET - a database of gene-disease associations

Cohen syndrome, C0265223

Variant: rs386834078 ×

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:

rs386834078

VPS13B

0.700

GeneticVariation

CLINVAR

Using whole-exome sequencing to identify inherited causes of autism.

23352163

2013

dbSNP:

rs386834078

VPS13B

0.700

GeneticVariation

CLINVAR

Delineation of Cohen syndrome following a large-scale genotype-phenotype screen.

15141358

2004