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rs2942168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs2942168(C;C)
Make rs2942168(C;T)
Make rs2942168(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position45637484
GeneCRHR1, DBC1
is asnp
is mentioned by
dbSNPrs2942168
ebirs2942168
HLIrs2942168
Exacrs2942168
Varsomers2942168
Maprs2942168
PheGenIrs2942168
hapmaprs2942168
1000 genomesrs2942168
hgdprs2942168
ensemblrs2942168
gopubmedrs2942168
geneviewrs2942168
scholarrs2942168
googlers2942168
pharmgkbrs2942168
gwascentralrs2942168
openSNPrs2942168
23andMers2942168
23andMe allrs2942168
SNP Nexus

SNPshotrs2942168
SNPdbers2942168
MSV3drs2942168
GWAS Ctlgrs2942168
GMAF0.1162
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 G
P-val 1E-28
Odds Ratio 1.2700 [1.23-1.31]


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