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rs10501570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 1 Normal risk of developing Parkinson's Disease
Make rs10501570(C;C)
Make rs10501570(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position84706803
GeneDLG2
is asnp
is mentioned by
dbSNPrs10501570
ebirs10501570
HLIrs10501570
Exacrs10501570
Varsomers10501570
Maprs10501570
PheGenIrs10501570
hapmaprs10501570
1000 genomesrs10501570
hgdprs10501570
ensemblrs10501570
gopubmedrs10501570
geneviewrs10501570
scholarrs10501570
googlers10501570
pharmgkbrs10501570
gwascentralrs10501570
openSNPrs10501570
23andMers10501570
23andMe allrs10501570
SNP Nexus

SNPshotrs10501570
SNPdbers10501570
MSV3drs10501570
GWAS Ctlgrs10501570
GMAF0.09734
Max Magnitude1
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10501570
PubMedID [PMID 17052657]
Condition Parkinson's disease
Gene DLG2
Risk Allele
pValue 7.00E-006
OR 5
95% CI 2.00-12.50



[PMID 19208180OA-icon.png] Detecting disease-associated genotype patterns.

[PMID 19429005OA-icon.png] Phactr2 and Parkinson's disease.


GET Evidence
rs10501570
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary