DisGeNET - a database of gene-disease associations

Dystrophia myotonica 2, C2931689

Variant: rs1871922 ×

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:

rs1871922

rs1871922

CNBP ; LOC105374101

0.010

GeneticVariation

BEFREE

In addition, the single-nucleotide polymorphism (SNP) rs1871922 located in the first intron of DM2 was genotyped.

2011