rs7931462
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs7931462(A;A) |
Make rs7931462(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 93051037 |
Gene | RPL26P31 |
is a | snp |
is | mentioned by |
dbSNP | rs7931462 |
dbSNP (classic) | rs7931462 |
ClinGen | rs7931462 |
ebi | rs7931462 |
HLI | rs7931462 |
Exac | rs7931462 |
Gnomad | rs7931462 |
Varsome | rs7931462 |
LitVar | rs7931462 |
Map | rs7931462 |
PheGenI | rs7931462 |
Biobank | rs7931462 |
1000 genomes | rs7931462 |
hgdp | rs7931462 |
ensembl | rs7931462 |
geneview | rs7931462 |
scholar | rs7931462 |
rs7931462 | |
pharmgkb | rs7931462 |
gwascentral | rs7931462 |
openSNP | rs7931462 |
23andMe | rs7931462 |
SNPshot | rs7931462 |
SNPdbe | rs7931462 |
MSV3d | rs7931462 |
GWAS Ctlg | rs7931462 |
GMAF | 0.03719 |
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 | G |
P-val | 2E-9 |
Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d