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rs10743889

From SNPedia

Orientationplus
Stabilizedplus
Make rs10743889(G;G)
Make rs10743889(G;T)
Make rs10743889(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position10368790
GeneLOC101928100
is asnp
is mentioned by
dbSNPrs10743889
dbSNP (classic)rs10743889
ClinGenrs10743889
ebirs10743889
HLIrs10743889
Exacrs10743889
Gnomadrs10743889
Varsomers10743889
LitVarrs10743889
Maprs10743889
PheGenIrs10743889
Biobankrs10743889
1000 genomesrs10743889
hgdprs10743889
ensemblrs10743889
geneviewrs10743889
scholarrs10743889
googlers10743889
pharmgkbrs10743889
gwascentralrs10743889
openSNPrs10743889
23andMers10743889
SNPshotrs10743889
SNPdbers10743889
MSV3drs10743889
GWAS Ctlgrs10743889
GMAF0.241
Max Magnitude0
? (G;G) (G;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 C
P-val 6E-6
Odds Ratio .04 [NR] mL/min increase