DisGeNET - a database of gene-disease associations

LRRTM2, leucine rich repeat transmembrane neuronal 2, 26045

N. diseases: 1; N. variants: 1

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs11744283

rs11744283

Entrez Id:	1495;26045
Gene Symbol:	CTNNA1;LRRTM2

CTNNA1;LRRTM2

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

G

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

2017