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rs7520966

From SNPedia

Orientationplus
Stabilizedplus
Make rs7520966(C;C)
Make rs7520966(C;T)
Make rs7520966(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position54179589
GeneCYB5RL
is asnp
is mentioned by
dbSNPrs7520966
ebirs7520966
HLIrs7520966
Exacrs7520966
Varsomers7520966
Maprs7520966
PheGenIrs7520966
hapmaprs7520966
1000 genomesrs7520966
hgdprs7520966
ensemblrs7520966
gopubmedrs7520966
geneviewrs7520966
scholarrs7520966
googlers7520966
pharmgkbrs7520966
gwascentralrs7520966
openSNPrs7520966
23andMers7520966
23andMe allrs7520966
SNP Nexus

SNPshotrs7520966
SNPdbers7520966
MSV3drs7520966
GWAS Ctlgrs7520966
GMAF0.3343
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM606852
DescPARKINSON DISEASE 10; PARK10
Variant
Relatedalso
[PMID 16252231OA-icon.png] High-resolution whole-genome association study of Parkinson disease.


[PMID 16685661OA-icon.png] Genomewide association, Parkinson disease, and PARK10.


[PMID 16685662OA-icon.png] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.


[PMID 16685663OA-icon.png] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.


[PMID 17052658OA-icon.png] Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.


[PMID 17332845OA-icon.png] Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.