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rs967582

From SNPedia

Orientationminus
Stabilizedminus
Make rs967582(G;G)
Make rs967582(G;T)
Make rs967582(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position50116500
GeneELAVL4
is asnp
is mentioned by
dbSNPrs967582
ebirs967582
HLIrs967582
Exacrs967582
Varsomers967582
Maprs967582
PheGenIrs967582
hapmaprs967582
1000 genomesrs967582
hgdprs967582
ensemblrs967582
gopubmedrs967582
geneviewrs967582
scholarrs967582
googlers967582
pharmgkbrs967582
gwascentralrs967582
openSNPrs967582
23andMers967582
23andMe allrs967582
SNP Nexus

SNPshotrs967582
SNPdbers967582
MSV3drs967582
GWAS Ctlgrs967582
GMAF0.4894
Max Magnitude
? (G;G) (G;T) (T;T) 28
OMIM606852
DescPARKINSON DISEASE 10; PARK10
Variant
Relatedalso
[PMID 15986317OA-icon.png] Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.


[PMID 17230446] ELAVL4, PARK10, and the Celts.


[PMID 18587682OA-icon.png] Replication of association between ELAVL4 and Parkinson disease: the GenePD study.