rs11737074
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11737074(A;A) |
Make rs11737074(A;G) |
Make rs11737074(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 124160218 |
Gene | LOC105377407 |
is a | snp |
is | mentioned by |
dbSNP | rs11737074 |
dbSNP (classic) | rs11737074 |
ClinGen | rs11737074 |
ebi | rs11737074 |
HLI | rs11737074 |
Exac | rs11737074 |
Gnomad | rs11737074 |
Varsome | rs11737074 |
LitVar | rs11737074 |
Map | rs11737074 |
PheGenI | rs11737074 |
Biobank | rs11737074 |
1000 genomes | rs11737074 |
hgdp | rs11737074 |
ensembl | rs11737074 |
geneview | rs11737074 |
scholar | rs11737074 |
rs11737074 | |
pharmgkb | rs11737074 |
gwascentral | rs11737074 |
openSNP | rs11737074 |
23andMe | rs11737074 |
SNPshot | rs11737074 |
SNPdbe | rs11737074 |
MSV3d | rs11737074 |
GWAS Ctlg | rs11737074 |
GMAF | 0.14 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs11737074 increases susceptibility to Parkinson's disease 1.50 times for carriers of the A allele [PMID 16252231]
[PMID 16685661] Genomewide association, Parkinson disease, and PARK10.
[PMID 16685662] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
[PMID 16685663] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.