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rs10433903

From SNPedia

Orientationplus
Stabilizedplus
Make rs10433903(C;C)
Make rs10433903(C;T)
Make rs10433903(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position117171981
is asnp
is mentioned by
dbSNPrs10433903
ebirs10433903
HLIrs10433903
Exacrs10433903
Varsomers10433903
Maprs10433903
PheGenIrs10433903
hapmaprs10433903
1000 genomesrs10433903
hgdprs10433903
ensemblrs10433903
gopubmedrs10433903
geneviewrs10433903
scholarrs10433903
googlers10433903
pharmgkbrs10433903
gwascentralrs10433903
openSNPrs10433903
23andMers10433903
23andMe allrs10433903
SNP Nexus

SNPshotrs10433903
SNPdbers10433903
MSV3drs10433903
GWAS Ctlgrs10433903
GMAF0.3737
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele T
P-val 0.000003
Odds Ratio 1.33 [1.19-1.52]


GET Evidence
rs10433903
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.277778
summary