rs10012307
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10012307(C;C) |
Make rs10012307(C;T) |
Make rs10012307(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 136605429 |
is a | snp |
is | mentioned by |
dbSNP | rs10012307 |
dbSNP (classic) | rs10012307 |
ClinGen | rs10012307 |
ebi | rs10012307 |
HLI | rs10012307 |
Exac | rs10012307 |
Gnomad | rs10012307 |
Varsome | rs10012307 |
LitVar | rs10012307 |
Map | rs10012307 |
PheGenI | rs10012307 |
Biobank | rs10012307 |
1000 genomes | rs10012307 |
hgdp | rs10012307 |
ensembl | rs10012307 |
geneview | rs10012307 |
scholar | rs10012307 |
rs10012307 | |
pharmgkb | rs10012307 |
gwascentral | rs10012307 |
openSNP | rs10012307 |
23andMe | rs10012307 |
SNPshot | rs10012307 |
SNPdbe | rs10012307 |
MSV3d | rs10012307 |
GWAS Ctlg | rs10012307 |
GMAF | 0.2672 |
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 | T |
P-val | 2E-8 |
Odds Ratio | NR NR |