rs10513789
From SNPedia
Orientation | plus |
Stabilized | plus |
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. |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 183042285 |
Gene | MCCC1 |
is a | snp |
is | mentioned by |
dbSNP | rs10513789 |
dbSNP (classic) | rs10513789 |
ClinGen | rs10513789 |
ebi | rs10513789 |
HLI | rs10513789 |
Exac | rs10513789 |
Gnomad | rs10513789 |
Varsome | rs10513789 |
LitVar | rs10513789 |
Map | rs10513789 |
PheGenI | rs10513789 |
Biobank | rs10513789 |
1000 genomes | rs10513789 |
hgdp | rs10513789 |
ensembl | rs10513789 |
geneview | rs10513789 |
scholar | rs10513789 |
rs10513789 | |
pharmgkb | rs10513789 |
gwascentral | rs10513789 |
openSNP | rs10513789 |
23andMe | rs10513789 |
SNPshot | rs10513789 |
SNPdbe | rs10513789 |
MSV3d | rs10513789 |
GWAS Ctlg | rs10513789 |
GMAF | 0.3264 |
Max Magnitude | 1.8 |
? | (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 21738487]
23andMe has a patent covering this snp. http://blog.23andme.com/2012/05/28/announcing-23andmes-first-patent/