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rs7336332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7336332(A;G)
Make rs7336332(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27484267
is asnp
is mentioned by
dbSNPrs7336332
ebirs7336332
HLIrs7336332
Exacrs7336332
Varsomers7336332
Maprs7336332
PheGenIrs7336332
hapmaprs7336332
1000 genomesrs7336332
hgdprs7336332
ensemblrs7336332
gopubmedrs7336332
geneviewrs7336332
scholarrs7336332
googlers7336332
pharmgkbrs7336332
gwascentralrs7336332
openSNPrs7336332
23andMers7336332
23andMe allrs7336332
SNP Nexus

SNPshotrs7336332
SNPdbers7336332
MSV3drs7336332
GWAS Ctlgrs7336332
GMAF0.1832
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19079260]
Trait Weight
Title Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Risk Allele G
P-val 0.000001
Odds Ratio 4.01 [2.40-5.62] % SD



GET Evidence
rs7336332
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary