DisGeNET - a database of gene-disease associations

Pituitary Dwarfism Type 3, C0878683

Variant: rs587776682 ×

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:

rs587776682

rs587776682

PROP1

G

0.700

CausalMutation

CLINVAR

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

2005

dbSNP:

rs587776682

rs587776682

PROP1

G

0.700

GeneticVariation

CLINVAR