rs2073376
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2073376(A;G) |
Make rs2073376(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 46431839 |
Gene | PCNT |
is a | snp |
is | mentioned by |
dbSNP | rs2073376 |
dbSNP (classic) | rs2073376 |
ClinGen | rs2073376 |
ebi | rs2073376 |
HLI | rs2073376 |
Exac | rs2073376 |
Gnomad | rs2073376 |
Varsome | rs2073376 |
LitVar | rs2073376 |
Map | rs2073376 |
PheGenI | rs2073376 |
Biobank | rs2073376 |
1000 genomes | rs2073376 |
hgdp | rs2073376 |
ensembl | rs2073376 |
geneview | rs2073376 |
scholar | rs2073376 |
rs2073376 | |
pharmgkb | rs2073376 |
gwascentral | rs2073376 |
openSNP | rs2073376 |
23andMe | rs2073376 |
SNPshot | rs2073376 |
SNPdbe | rs2073376 |
MSV3d | rs2073376 |
GWAS Ctlg | rs2073376 |
GMAF | 0.3237 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19448849] Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population
ClinVar | |
---|---|
Risk | rs2073376(G;G) |
Alt | rs2073376(G;G) |
Reference | Rs2073376(A;A) |
Significance | Non-pathogenic |
Disease | not specified Microcephalic Osteodysplastic Primordial Dwarfism |
Variation | info |
Gene | PCNT |
CLNDBN | not specified Microcephalic Osteodysplastic Primordial Dwarfism |
Reversed | 0 |
HGVS | NC_000021.8:g.47851753A>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000147222.4, RCV000329338.1, |