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rs4837628

From SNPedia

Orientationplus
Stabilizedplus
Make rs4837628(C;C)
Make rs4837628(C;T)
Make rs4837628(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position119297431
GeneBRINP1
is asnp
is mentioned by
dbSNPrs4837628
ebirs4837628
HLIrs4837628
Exacrs4837628
Varsomers4837628
Maprs4837628
PheGenIrs4837628
hapmaprs4837628
1000 genomesrs4837628
hgdprs4837628
ensemblrs4837628
gopubmedrs4837628
geneviewrs4837628
scholarrs4837628
googlers4837628
pharmgkbrs4837628
gwascentralrs4837628
openSNPrs4837628
23andMers4837628
23andMe allrs4837628
SNP Nexus

SNPshotrs4837628
SNPdbers4837628
MSV3drs4837628
GWAS Ctlgrs4837628
GMAF0.4412
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20070850OA-icon.png]
Trait Parkinson's disease
Title Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Risk Allele A
P-val 0.000001
Odds Ratio 1.27 [1.15-1.39]