rs4819833
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4819833(C;C) |
Make rs4819833(C;T) |
Make rs4819833(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 19703979 |
is a | snp |
is | mentioned by |
dbSNP | rs4819833 |
dbSNP (classic) | rs4819833 |
ClinGen | rs4819833 |
ebi | rs4819833 |
HLI | rs4819833 |
Exac | rs4819833 |
Gnomad | rs4819833 |
Varsome | rs4819833 |
LitVar | rs4819833 |
Map | rs4819833 |
PheGenI | rs4819833 |
Biobank | rs4819833 |
1000 genomes | rs4819833 |
hgdp | rs4819833 |
ensembl | rs4819833 |
geneview | rs4819833 |
scholar | rs4819833 |
rs4819833 | |
pharmgkb | rs4819833 |
gwascentral | rs4819833 |
openSNP | rs4819833 |
23andMe | rs4819833 |
SNPshot | rs4819833 |
SNPdbe | rs4819833 |
MSV3d | rs4819833 |
GWAS Ctlg | rs4819833 |
GMAF | 0.3421 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23725790] |
Trait | DNA methylation (parent-of-origin) |
Title | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. |
Risk Allele | C |
P-val | 6E-8 |
Odds Ratio | NR NR |