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rs2655898

From SNPedia

Orientationminus
Stabilizedminus
Make rs2655898(A;A)
Make rs2655898(A;G)
Make rs2655898(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position60416871
is asnp
is mentioned by
dbSNPrs2655898
dbSNP (classic)rs2655898
ClinGenrs2655898
ebirs2655898
HLIrs2655898
Exacrs2655898
Gnomadrs2655898
Varsomers2655898
LitVarrs2655898
Maprs2655898
PheGenIrs2655898
Biobankrs2655898
1000 genomesrs2655898
hgdprs2655898
ensemblrs2655898
geneviewrs2655898
scholarrs2655898
googlers2655898
pharmgkbrs2655898
gwascentralrs2655898
openSNPrs2655898
23andMers2655898
SNPshotrs2655898
SNPdbers2655898
MSV3drs2655898
GWAS Ctlgrs2655898
GMAF0.3494
Max Magnitude0
? (A;A) (A;G) (G;G) 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 8E-6
Odds Ratio .03 [NR] kcal/d increase