rs9883474
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9883474(A;A) |
Make rs9883474(A;C) |
Make rs9883474(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 87476299 |
is a | snp |
is | mentioned by |
dbSNP | rs9883474 |
dbSNP (classic) | rs9883474 |
ClinGen | rs9883474 |
ebi | rs9883474 |
HLI | rs9883474 |
Exac | rs9883474 |
Gnomad | rs9883474 |
Varsome | rs9883474 |
LitVar | rs9883474 |
Map | rs9883474 |
PheGenI | rs9883474 |
Biobank | rs9883474 |
1000 genomes | rs9883474 |
hgdp | rs9883474 |
ensembl | rs9883474 |
geneview | rs9883474 |
scholar | rs9883474 |
rs9883474 | |
pharmgkb | rs9883474 |
gwascentral | rs9883474 |
openSNP | rs9883474 |
23andMe | rs9883474 |
SNPshot | rs9883474 |
SNPdbe | rs9883474 |
MSV3d | rs9883474 |
GWAS Ctlg | rs9883474 |
GMAF | 0.1492 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23471985] |
Trait | Brain connectivity |
Title | Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. |
Risk Allele | |
P-val | 3E-9 |
Odds Ratio | NR NR |