DisGeNET - a database of gene-disease associations

Parkinsonian Disorders, C0242422

Variant: rs121908683 ×

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:

rs121908683

rs121908683

PLA2G6

0.010

GeneticVariation

BEFREE

Here, we report the segregation of R632W with disease in an Iranian consanguineous dystonia-parkinsonism pedigree.

2009