rs7077361
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs7077361(C;C) |
Make rs7077361(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 15519544 |
Gene | ITGA8 |
is a | snp |
is | mentioned by |
dbSNP | rs7077361 |
dbSNP (classic) | rs7077361 |
ClinGen | rs7077361 |
ebi | rs7077361 |
HLI | rs7077361 |
Exac | rs7077361 |
Gnomad | rs7077361 |
Varsome | rs7077361 |
LitVar | rs7077361 |
Map | rs7077361 |
PheGenI | rs7077361 |
Biobank | rs7077361 |
1000 genomes | rs7077361 |
hgdp | rs7077361 |
ensembl | rs7077361 |
geneview | rs7077361 |
scholar | rs7077361 |
rs7077361 | |
pharmgkb | rs7077361 |
gwascentral | rs7077361 |
openSNP | rs7077361 |
23andMe | rs7077361 |
SNPshot | rs7077361 |
SNPdbe | rs7077361 |
MSV3d | rs7077361 |
GWAS Ctlg | rs7077361 |
GMAF | 0.06244 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19915575] |
Trait | Parkinson's disease |
Title | Genome-wide association study reveals genetic risk underlying Parkinson's disease |
Risk Allele | C |
P-val | 0.000005 |
Odds Ratio | 1.19 [NR] |