DisGeNET - a database of gene-disease associations

Night blindness, congenital stationary, C0339535

Variant: rs122456134 ×

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

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs122456134

rs122456134

CACNA1F

A

0.700

CausalMutation

CLINVAR

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

1998