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rs7671189

From SNPedia

Orientationplus
Stabilizedplus
Make rs7671189(C;C)
Make rs7671189(C;T)
Make rs7671189(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position11673037
GeneLOC107986178
is asnp
is mentioned by
dbSNPrs7671189
dbSNP (classic)rs7671189
ClinGenrs7671189
ebirs7671189
HLIrs7671189
Exacrs7671189
Gnomadrs7671189
Varsomers7671189
LitVarrs7671189
Maprs7671189
PheGenIrs7671189
Biobankrs7671189
1000 genomesrs7671189
hgdprs7671189
ensemblrs7671189
geneviewrs7671189
scholarrs7671189
googlers7671189
pharmgkbrs7671189
gwascentralrs7671189
openSNPrs7671189
23andMers7671189
SNPshotrs7671189
SNPdbers7671189
MSV3drs7671189
GWAS Ctlgrs7671189
GMAF0.2805
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 A
P-val 3E-6
Odds Ratio .03 [NR] nmol/L increase