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rs16961557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs16961557(A;G)
Make rs16961557(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48755931
GeneCEP152
is asnp
is mentioned by
dbSNPrs16961557
ebirs16961557
HLIrs16961557
Exacrs16961557
Varsomers16961557
Maprs16961557
PheGenIrs16961557
hapmaprs16961557
1000 genomesrs16961557
hgdprs16961557
ensemblrs16961557
gopubmedrs16961557
geneviewrs16961557
scholarrs16961557
googlers16961557
pharmgkbrs16961557
gwascentralrs16961557
openSNPrs16961557
23andMers16961557
23andMe allrs16961557
SNP Nexus

SNPshotrs16961557
SNPdbers16961557
MSV3drs16961557
GWAS Ctlgrs16961557
GMAF0.03168
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 5E-6
Odds Ratio .03 [NR] cm increase


ClinVar
Risk rs16961557(G;G)
Alt rs16961557(G;G)
Reference rs16961557(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CEP152
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.49048128A>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000145626.1,