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rs6907728

From SNPedia

Orientationplus
Stabilizedplus
Make rs6907728(A;A)
Make rs6907728(A;C)
Make rs6907728(C;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position131907629
is asnp
is mentioned by
dbSNPrs6907728
dbSNP (classic)rs6907728
ClinGenrs6907728
ebirs6907728
HLIrs6907728
Exacrs6907728
Gnomadrs6907728
Varsomers6907728
LitVarrs6907728
Maprs6907728
PheGenIrs6907728
Biobankrs6907728
1000 genomesrs6907728
hgdprs6907728
ensemblrs6907728
geneviewrs6907728
scholarrs6907728
googlers6907728
pharmgkbrs6907728
gwascentralrs6907728
openSNPrs6907728
23andMers6907728
SNPshotrs6907728
SNPdbers6907728
MSV3drs6907728
GWAS Ctlgrs6907728
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 3E-6
Odds Ratio .04 [NR] ng/mL increase