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rs6726292

From SNPedia

Orientationplus
Stabilizedplus
Make rs6726292(A;A)
Make rs6726292(A;G)
Make rs6726292(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position54929493
GeneEML6
is asnp
is mentioned by
dbSNPrs6726292
ebirs6726292
HLIrs6726292
Exacrs6726292
Varsomers6726292
Maprs6726292
PheGenIrs6726292
hapmaprs6726292
1000 genomesrs6726292
hgdprs6726292
ensemblrs6726292
gopubmedrs6726292
geneviewrs6726292
scholarrs6726292
googlers6726292
pharmgkbrs6726292
gwascentralrs6726292
openSNPrs6726292
23andMers6726292
23andMe allrs6726292
SNP Nexus

SNPshotrs6726292
SNPdbers6726292
MSV3drs6726292
GWAS Ctlgrs6726292
GMAF0.3044
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele G
P-val 0.000001
Odds Ratio 1.39 [1.22-1.59]


GET Evidence
rs6726292
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.373016
summary