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rs6532194

From SNPedia

Orientationplus
Stabilizedplus
Make rs6532194(C;C)
Make rs6532194(C;T)
Make rs6532194(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position89859751
is asnp
is mentioned by
dbSNPrs6532194
dbSNP (classic)rs6532194
ClinGenrs6532194
ebirs6532194
HLIrs6532194
Exacrs6532194
Gnomadrs6532194
Varsomers6532194
LitVarrs6532194
Maprs6532194
PheGenIrs6532194
Biobankrs6532194
1000 genomesrs6532194
hgdprs6532194
ensemblrs6532194
geneviewrs6532194
scholarrs6532194
googlers6532194
pharmgkbrs6532194
gwascentralrs6532194
openSNPrs6532194
23andMers6532194
SNPshotrs6532194
SNPdbers6532194
MSV3drs6532194
GWAS Ctlgrs6532194
GMAF0.3448
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22438815OA-icon.png]
Trait
Title Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
Risk Allele
P-val 5E-11
Odds Ratio 1.2900 None


[PMID 21268244] Association of GWAS loci with PD in China.