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rs10107366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common genotype
Make rs10107366(C;C)
Make rs10107366(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position98101459
GeneHRSP12
is asnp
is mentioned by
dbSNPrs10107366
dbSNP (classic)rs10107366
ClinGenrs10107366
ebirs10107366
HLIrs10107366
Exacrs10107366
Gnomadrs10107366
Varsomers10107366
LitVarrs10107366
Maprs10107366
PheGenIrs10107366
Biobankrs10107366
1000 genomesrs10107366
hgdprs10107366
ensemblrs10107366
geneviewrs10107366
scholarrs10107366
googlers10107366
pharmgkbrs10107366
gwascentralrs10107366
openSNPrs10107366
23andMers10107366
SNPshotrs10107366
SNPdbers10107366
MSV3drs10107366
GWAS Ctlgrs10107366
GMAF0.02342
Max Magnitude0
? (C;C) (C;T) (T;T) 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-7
Odds Ratio .04 [NR] kcal/d increase