rs7027203
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7027203(A;A) |
Make rs7027203(A;C) |
Make rs7027203(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 93800281 |
is a | snp |
is | mentioned by |
dbSNP | rs7027203 |
dbSNP (classic) | rs7027203 |
ClinGen | rs7027203 |
ebi | rs7027203 |
HLI | rs7027203 |
Exac | rs7027203 |
Gnomad | rs7027203 |
Varsome | rs7027203 |
LitVar | rs7027203 |
Map | rs7027203 |
PheGenI | rs7027203 |
Biobank | rs7027203 |
1000 genomes | rs7027203 |
hgdp | rs7027203 |
ensembl | rs7027203 |
geneview | rs7027203 |
scholar | rs7027203 |
rs7027203 | |
pharmgkb | rs7027203 |
gwascentral | rs7027203 |
openSNP | rs7027203 |
23andMe | rs7027203 |
SNPshot | rs7027203 |
SNPdbe | rs7027203 |
MSV3d | rs7027203 |
GWAS Ctlg | rs7027203 |
GMAF | 0.3067 |
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 | C |
P-val | 6E-6 |
Odds Ratio | NR NR |