rs11897432
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11897432(A;A) |
Make rs11897432(A;G) |
Make rs11897432(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 43590366 |
Gene | THADA |
is a | snp |
is | mentioned by |
dbSNP | rs11897432 |
dbSNP (classic) | rs11897432 |
ClinGen | rs11897432 |
ebi | rs11897432 |
HLI | rs11897432 |
Exac | rs11897432 |
Gnomad | rs11897432 |
Varsome | rs11897432 |
LitVar | rs11897432 |
Map | rs11897432 |
PheGenI | rs11897432 |
Biobank | rs11897432 |
1000 genomes | rs11897432 |
hgdp | rs11897432 |
ensembl | rs11897432 |
geneview | rs11897432 |
scholar | rs11897432 |
rs11897432 | |
pharmgkb | rs11897432 |
gwascentral | rs11897432 |
openSNP | rs11897432 |
23andMe | rs11897432 |
SNPshot | rs11897432 |
SNPdbe | rs11897432 |
MSV3d | rs11897432 |
GWAS Ctlg | rs11897432 |
GMAF | 0.1428 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 8E-7 |
Odds Ratio | NR NR |