rs514636
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs514636(A;G) |
Make rs514636(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 183152648 |
Gene | LAMP3 |
is a | snp |
is | mentioned by |
dbSNP | rs514636 |
dbSNP (classic) | rs514636 |
ClinGen | rs514636 |
ebi | rs514636 |
HLI | rs514636 |
Exac | rs514636 |
Gnomad | rs514636 |
Varsome | rs514636 |
LitVar | rs514636 |
Map | rs514636 |
PheGenI | rs514636 |
Biobank | rs514636 |
1000 genomes | rs514636 |
hgdp | rs514636 |
ensembl | rs514636 |
geneview | rs514636 |
scholar | rs514636 |
rs514636 | |
pharmgkb | rs514636 |
gwascentral | rs514636 |
openSNP | rs514636 |
23andMe | rs514636 |
SNPshot | rs514636 |
SNPdbe | rs514636 |
MSV3d | rs514636 |
GWAS Ctlg | rs514636 |
GMAF | 0.118 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21254220] |
Trait | |
Title | Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder. |
Risk Allele | |
P-val | 7E-7 |
Odds Ratio | None None |