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rs4771996

From SNPedia

Orientationplus
Stabilizedplus
Make rs4771996(A;A)
Make rs4771996(A;G)
Make rs4771996(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position97401538
is asnp
is mentioned by
dbSNPrs4771996
dbSNP (classic)rs4771996
ClinGenrs4771996
ebirs4771996
HLIrs4771996
Exacrs4771996
Gnomadrs4771996
Varsomers4771996
LitVarrs4771996
Maprs4771996
PheGenIrs4771996
Biobankrs4771996
1000 genomesrs4771996
hgdprs4771996
ensemblrs4771996
geneviewrs4771996
scholarrs4771996
googlers4771996
pharmgkbrs4771996
gwascentralrs4771996
openSNPrs4771996
23andMers4771996
SNPshotrs4771996
SNPdbers4771996
MSV3drs4771996
GWAS Ctlgrs4771996
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele G
P-val 6E-6
Odds Ratio .03 [NR] cm increase