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rs6710823

From SNPedia

Orientationplus
Stabilizedplus
Make rs6710823(A;A)
Make rs6710823(A;G)
Make rs6710823(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position134834811
is asnp
is mentioned by
dbSNPrs6710823
ebirs6710823
HLIrs6710823
Exacrs6710823
Varsomers6710823
Maprs6710823
PheGenIrs6710823
hapmaprs6710823
1000 genomesrs6710823
hgdprs6710823
ensemblrs6710823
gopubmedrs6710823
geneviewrs6710823
scholarrs6710823
googlers6710823
pharmgkbrs6710823
gwascentralrs6710823
openSNPrs6710823
23andMers6710823
23andMe allrs6710823
SNP Nexus

SNPshotrs6710823
SNPdbers6710823
MSV3drs6710823
GWAS Ctlgrs6710823
GMAF0.1786
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 7E-9
Odds Ratio 1.1000 [1.06-1.14]