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rs7723605

From SNPedia

Orientationplus
Stabilizedplus
Make rs7723605(C;C)
Make rs7723605(C;T)
Make rs7723605(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position5354502
is asnp
is mentioned by
dbSNPrs7723605
ebirs7723605
HLIrs7723605
Exacrs7723605
Varsomers7723605
Maprs7723605
PheGenIrs7723605
hapmaprs7723605
1000 genomesrs7723605
hgdprs7723605
ensemblrs7723605
gopubmedrs7723605
geneviewrs7723605
scholarrs7723605
googlers7723605
pharmgkbrs7723605
gwascentralrs7723605
openSNPrs7723605
23andMers7723605
23andMe allrs7723605
SNP Nexus

SNPshotrs7723605
SNPdbers7723605
MSV3drs7723605
GWAS Ctlgrs7723605
GMAF0.2695
Max Magnitude
? (C;C) (C;T) (T;T) 28

Originally reported to be one of 13 SNPs found in whole genome association study to be associated with Parkinson's disease. However, neither it (nor the other 13) appeared to be associated with Parkinson's disease in an independent study of 663 Caucasian patients.[PMID 18280617]

[PMID 16252231OA-icon.png] High-resolution whole-genome association study of Parkinson disease.

[PMID 16685661OA-icon.png] Genomewide association, Parkinson disease, and PARK10.

[PMID 16685662OA-icon.png] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

[PMID 16685663OA-icon.png] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.