DisGeNET - a database of gene-disease associations

Dystrophia myotonica 2, C2931689

Variant: rs699 ×

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:

rs699

rs699

AGT

0.010

GeneticVariation

BEFREE

Our results suggest that there is an association between the AGT rs699 polymorphism and DM2 in a Brazilian sample.

2015