rs2338971
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2338971(C;C) |
Make rs2338971(C;T) |
Make rs2338971(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 101414449 |
is a | snp |
is | mentioned by |
dbSNP | rs2338971 |
dbSNP (classic) | rs2338971 |
ClinGen | rs2338971 |
ebi | rs2338971 |
HLI | rs2338971 |
Exac | rs2338971 |
Gnomad | rs2338971 |
Varsome | rs2338971 |
LitVar | rs2338971 |
Map | rs2338971 |
PheGenI | rs2338971 |
Biobank | rs2338971 |
1000 genomes | rs2338971 |
hgdp | rs2338971 |
ensembl | rs2338971 |
geneview | rs2338971 |
scholar | rs2338971 |
rs2338971 | |
pharmgkb | rs2338971 |
gwascentral | rs2338971 |
openSNP | rs2338971 |
23andMe | rs2338971 |
SNPshot | rs2338971 |
SNPdbe | rs2338971 |
MSV3d | rs2338971 |
GWAS Ctlg | rs2338971 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24511991![]() |
Trait | Parkinson's disease |
Title | Identification of a novel Parkinson's disease locus via stratified genome-wide association study. |
Risk Allele | C |
P-val | 5E-10 |
Odds Ratio | 1.32 [1.26-1.38] |