DisGeNET - a database of gene-disease associations

Source: ALL

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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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Oculocutaneous albinism type 2

CUI:	C0268495
Disease:	Oculocutaneous albinism type 2

0.700

GeneticVariation

CLINVAR

Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population.

2015