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rs3902720

From SNPedia

Orientationplus
Stabilizedplus
Make rs3902720(C;C)
Make rs3902720(C;T)
Make rs3902720(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position50139665
GeneELAVL4
is asnp
is mentioned by
dbSNPrs3902720
ebirs3902720
HLIrs3902720
Exacrs3902720
Varsomers3902720
Maprs3902720
PheGenIrs3902720
hapmaprs3902720
1000 genomesrs3902720
hgdprs3902720
ensemblrs3902720
gopubmedrs3902720
geneviewrs3902720
scholarrs3902720
googlers3902720
pharmgkbrs3902720
gwascentralrs3902720
openSNPrs3902720
23andMers3902720
23andMe allrs3902720
SNP Nexus

SNPshotrs3902720
SNPdbers3902720
MSV3drs3902720
GWAS Ctlgrs3902720
GMAF0.477
Max Magnitude
? (C;C) (C;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.