rs476828
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs476828(A;A) |
Make rs476828(A;G) |
Make rs476828(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 60185354 |
is a | snp |
is | mentioned by |
dbSNP | rs476828 |
dbSNP (classic) | rs476828 |
ClinGen | rs476828 |
ebi | rs476828 |
HLI | rs476828 |
Exac | rs476828 |
Gnomad | rs476828 |
Varsome | rs476828 |
LitVar | rs476828 |
Map | rs476828 |
PheGenI | rs476828 |
Biobank | rs476828 |
1000 genomes | rs476828 |
hgdp | rs476828 |
ensembl | rs476828 |
geneview | rs476828 |
scholar | rs476828 |
rs476828 | |
pharmgkb | rs476828 |
gwascentral | rs476828 |
openSNP | rs476828 |
23andMe | rs476828 |
SNPshot | rs476828 |
SNPdbe | rs476828 |
MSV3d | rs476828 |
GWAS Ctlg | rs476828 |
GMAF | 0.2672 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19265794] Investigation of the Locus Near MC4R With Childhood Obesity in Americans of European and African Ancestry
[PMID 20421936] Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
GWAS snp | |
---|---|
PMID | [PMID 23563609] |
Trait | Obesity (early onset extreme) |
Title | Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. |
Risk Allele | C |
P-val | 9E-14 |
Odds Ratio | 1.33 [1.23-1.43] |
[PMID 32770936] The MC4R SNPs, their haplotypes and gene-environment interactions on the risk of obesity.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2d
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M