Have questions? Visit https://www.reddit.com/r/SNPedia

rs6430538

From SNPedia

Orientationplus
Stabilizedplus
Make rs6430538(C;C)
Make rs6430538(C;T)
Make rs6430538(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position134782397
is asnp
is mentioned by
dbSNPrs6430538
dbSNP (classic)rs6430538
ClinGenrs6430538
ebirs6430538
HLIrs6430538
Exacrs6430538
Gnomadrs6430538
Varsomers6430538
LitVarrs6430538
Maprs6430538
PheGenIrs6430538
Biobankrs6430538
1000 genomesrs6430538
hgdprs6430538
ensemblrs6430538
geneviewrs6430538
scholarrs6430538
googlers6430538
pharmgkbrs6430538
gwascentralrs6430538
openSNPrs6430538
23andMers6430538
SNPshotrs6430538
SNPdbers6430538
MSV3drs6430538
GWAS Ctlgrs6430538
GMAF0.2397
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22451204OA-icon.png]
Trait
Title Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Risk Allele
P-val 2E-7
Odds Ratio 1.1500 None


[PMID 31430546] A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population.