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rs11711441

From SNPedia

Orientationplus
Stabilizedplus
Make rs11711441(A;A)
Make rs11711441(A;G)
Make rs11711441(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position183103487
is asnp
is mentioned by
dbSNPrs11711441
ebirs11711441
HLIrs11711441
Exacrs11711441
Varsomers11711441
Maprs11711441
PheGenIrs11711441
hapmaprs11711441
1000 genomesrs11711441
hgdprs11711441
ensemblrs11711441
gopubmedrs11711441
geneviewrs11711441
scholarrs11711441
googlers11711441
pharmgkbrs11711441
gwascentralrs11711441
openSNPrs11711441
23andMers11711441
23andMe allrs11711441
SNP Nexus

SNPshotrs11711441
SNPdbers11711441
MSV3drs11711441
GWAS Ctlgrs11711441
GMAF0.1433
Max Magnitude
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 8E-12
Odds Ratio 1.1900 [1.13-1.25]

[PMID 23496138] MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese.