rs3763558
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3763558(A;A) |
Make rs3763558(A;C) |
Make rs3763558(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 96784503 |
Gene | CPQ |
is a | snp |
is | mentioned by |
dbSNP | rs3763558 |
dbSNP (classic) | rs3763558 |
ClinGen | rs3763558 |
ebi | rs3763558 |
HLI | rs3763558 |
Exac | rs3763558 |
Gnomad | rs3763558 |
Varsome | rs3763558 |
LitVar | rs3763558 |
Map | rs3763558 |
PheGenI | rs3763558 |
Biobank | rs3763558 |
1000 genomes | rs3763558 |
hgdp | rs3763558 |
ensembl | rs3763558 |
geneview | rs3763558 |
scholar | rs3763558 |
rs3763558 | |
pharmgkb | rs3763558 |
gwascentral | rs3763558 |
openSNP | rs3763558 |
23andMe | rs3763558 |
SNPshot | rs3763558 |
SNPdbe | rs3763558 |
MSV3d | rs3763558 |
GWAS Ctlg | rs3763558 |
GMAF | 0.1474 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23725790] |
Trait | DNA methylation (variation) |
Title | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. |
Risk Allele | A |
P-val | 1E-6 |
Odds Ratio | NR NR |