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rs10513789

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 1.8 0.64x decreased risk of Parkinson's disease
(G;T) 1.4 0.8x decreased risk of Parkinson's disease
(T;T) 1.25 Very common. Normal risk of Parkinson's disease.
ReferenceGRCh38 38.1/141
Chromosome3
Position183042285
GeneMCCC1
is asnp
is mentioned by
dbSNPrs10513789
dbSNP (classic)rs10513789
ClinGenrs10513789
ebirs10513789
HLIrs10513789
Exacrs10513789
Gnomadrs10513789
Varsomers10513789
LitVarrs10513789
Maprs10513789
PheGenIrs10513789
Biobankrs10513789
1000 genomesrs10513789
hgdprs10513789
ensemblrs10513789
geneviewrs10513789
scholarrs10513789
googlers10513789
pharmgkbrs10513789
gwascentralrs10513789
openSNPrs10513789
23andMers10513789
SNPshotrs10513789
SNPdbers10513789
MSV3drs10513789
GWAS Ctlgrs10513789
GMAF0.3264
Max Magnitude1.8
? (G;G) (G;T) (T;T) 28


23andMe reports that the G allele of rs10513789 is associated with 0.8 times lower odds of Parkinson's disease. [PMID 21738487OA-icon.png]

23andMe has a patent covering this snp. http://blog.23andme.com/2012/05/28/announcing-23andmes-first-patent/

See also gs249 and gs248