DisGeNET - a database of gene-disease associations

Hirschsprung Disease, C0019569

Variant: rs7834206 ×

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:

rs7834206

rs7834206

NRG1

0.010

GeneticVariation

BEFREE

Furthermore, the rs7834206 polymorphism was associated with HSCR by case-control analysis (p = 0.037).

2018