DisGeNET - a database of gene-disease associations

Parkinson Disease, C0030567

Variant: rs3836790 ×

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:

rs3836790

rs3836790

SLC6A3

0.010

GeneticVariation

BEFREE

Our data suggest that variants rs28363170 and rs3836790 are not associated with sporadic PD in Han Chinese population.

2016