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rs476828

From SNPedia

Orientationminus
Stabilizedminus
Make rs476828(A;A)
Make rs476828(A;G)
Make rs476828(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position60185354
is asnp
is mentioned by
dbSNPrs476828
ebirs476828
HLIrs476828
Exacrs476828
Varsomers476828
Maprs476828
PheGenIrs476828
hapmaprs476828
1000 genomesrs476828
hgdprs476828
ensemblrs476828
gopubmedrs476828
geneviewrs476828
scholarrs476828
googlers476828
pharmgkbrs476828
gwascentralrs476828
openSNPrs476828
23andMers476828
23andMe allrs476828
SNP Nexus

SNPshotrs476828
SNPdbers476828
MSV3drs476828
GWAS Ctlgrs476828
GMAF0.2672
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19265794OA-icon.png] Investigation of the Locus Near MC4R With Childhood Obesity in Americans of European and African Ancestry


[PMID 20421936OA-icon.png] 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 23563609OA-icon.png]
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]