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rs34372695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34372695(C;T)
Make rs34372695(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156060246
GeneRAB25
is asnp
is mentioned by
dbSNPrs34372695
ebirs34372695
HLIrs34372695
Exacrs34372695
Varsomers34372695
Maprs34372695
PheGenIrs34372695
hapmaprs34372695
1000 genomesrs34372695
hgdprs34372695
ensemblrs34372695
gopubmedrs34372695
geneviewrs34372695
scholarrs34372695
googlers34372695
pharmgkbrs34372695
gwascentralrs34372695
openSNPrs34372695
23andMers34372695
23andMe allrs34372695
SNP Nexus

SNPshotrs34372695
SNPdbers34372695
MSV3drs34372695
GWAS Ctlgrs34372695
GMAF0.01286
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21292315OA-icon.png]
Trait
Title Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Risk Allele T
P-val 4E-12
Odds Ratio 1.4700 [1.35-1.59]


[PMID 22786590OA-icon.png] Large-scale replication and heterogeneity in Parkinson disease genetic loci