DisGeNET - a database of gene-disease associations

ROR2, receptor tyrosine kinase like orphan receptor 2, 4920

N. diseases: 250; N. variants: 20

Disease: Arthrogryposis ×

Variant: rs145631389 ×

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

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs145631389

rs145631389

Entrez Id:	4920
Gene Symbol:	ROR2

ROR2

CUI:	C0003886
Disease:

Arthrogryposis

C

0.700

GeneticVariation

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