rs10497324
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10497324(A;A) |
Make rs10497324(A;G) |
Make rs10497324(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 167302841 |
Gene | B3GALT1 |
is a | snp |
is | mentioned by |
dbSNP | rs10497324 |
dbSNP (classic) | rs10497324 |
ClinGen | rs10497324 |
ebi | rs10497324 |
HLI | rs10497324 |
Exac | rs10497324 |
Gnomad | rs10497324 |
Varsome | rs10497324 |
LitVar | rs10497324 |
Map | rs10497324 |
PheGenI | rs10497324 |
Biobank | rs10497324 |
1000 genomes | rs10497324 |
hgdp | rs10497324 |
ensembl | rs10497324 |
geneview | rs10497324 |
scholar | rs10497324 |
rs10497324 | |
pharmgkb | rs10497324 |
gwascentral | rs10497324 |
openSNP | rs10497324 |
23andMe | rs10497324 |
SNPshot | rs10497324 |
SNPdbe | rs10497324 |
MSV3d | rs10497324 |
GWAS Ctlg | rs10497324 |
GMAF | 0.08907 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 2E-9 |
Odds Ratio | NR NR |