DisGeNET - a database of gene-disease associations

Retinoblastoma, C0035335

Variant: rs587776783 ×

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:

rs587776783

RB1 ; LOC112268118

0.700

CausalMutation

CLINVAR

Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.

27582626

2016

dbSNP:

rs587776783

RB1 ; LOC112268118

0.700

CausalMutation

CLINVAR

Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.

26396485

2015

dbSNP:

rs587776783

RB1 ; LOC112268118

0.700

CausalMutation

CLINVAR

Genotype-phenotype correlations in hereditary familial retinoblastoma.

17096365

2007

dbSNP:

rs587776783

RB1 ; LOC112268118

0.700

CausalMutation

CLINVAR

Mutations in the RB1 gene and their effects on transcription.

2601691

1989