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rs10189050

From SNPedia

Orientationplus
Stabilizedplus
Make rs10189050(A;A)
Make rs10189050(A;C)
Make rs10189050(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position22901686
is asnp
is mentioned by
dbSNPrs10189050
dbSNP (classic)rs10189050
ClinGenrs10189050
ebirs10189050
HLIrs10189050
Exacrs10189050
Gnomadrs10189050
Varsomers10189050
LitVarrs10189050
Maprs10189050
PheGenIrs10189050
Biobankrs10189050
1000 genomesrs10189050
hgdprs10189050
ensemblrs10189050
geneviewrs10189050
scholarrs10189050
googlers10189050
pharmgkbrs10189050
gwascentralrs10189050
openSNPrs10189050
23andMers10189050
SNPshotrs10189050
SNPdbers10189050
MSV3drs10189050
GWAS Ctlgrs10189050
GMAF0.04867
Max Magnitude0
? (A;A) (A;C) (C;C) 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 C
P-val 4E-6
Odds Ratio .03 [NR] min/d increase