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rs9900972

From SNPedia

Orientationplus
Stabilizedplus
Make rs9900972(A;A)
Make rs9900972(A;G)
Make rs9900972(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position78872532
GeneTIMP2
is asnp
is mentioned by
dbSNPrs9900972
ebirs9900972
HLIrs9900972
Exacrs9900972
Varsomers9900972
Maprs9900972
PheGenIrs9900972
hapmaprs9900972
1000 genomesrs9900972
hgdprs9900972
ensemblrs9900972
gopubmedrs9900972
geneviewrs9900972
scholarrs9900972
googlers9900972
pharmgkbrs9900972
gwascentralrs9900972
openSNPrs9900972
23andMers9900972
23andMe allrs9900972
SNP Nexus

SNPshotrs9900972
SNPdbers9900972
MSV3drs9900972
GWAS Ctlgrs9900972
GMAF0.2874
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 18469019] rs6996321 significantly related to spine bone mineral density (p=0.002) and rs10914367 associated with hip BMD (p=0.028). Non-vertebral fracture risk was significantly increased in carriers of 'A' allele of rs9900972 (OR=2.06, p=0.0187)

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 8E-6
Odds Ratio .02 [NR] cm increase