DisGeNET - a database of gene-disease associations

rs10501920, CNTN5

N. diseases: 3

Disease: Atrial Fibrillation ×

Source: ALL

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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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Atrial Fibrillation

CUI:	C0004238
Disease:	Atrial Fibrillation

0.010

GeneticVariation

BEFREE

Also, rs10501920 in CNTN5 was associated with AF (p = 9.4 x 10(-6)) and HF (p = 1.2 x 10(-4)).

2007