Have questions? Visit https://www.reddit.com/r/SNPedia

rs999943

From SNPedia

Orientationminus
Stabilizedminus
Make rs999943(C;C)
Make rs999943(C;T)
Make rs999943(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position33656956
GeneITPR3
is asnp
is mentioned by
dbSNPrs999943
ebirs999943
HLIrs999943
Exacrs999943
Varsomers999943
Maprs999943
PheGenIrs999943
hapmaprs999943
1000 genomesrs999943
hgdprs999943
ensemblrs999943
gopubmedrs999943
geneviewrs999943
scholarrs999943
googlers999943
pharmgkbrs999943
gwascentralrs999943
openSNPrs999943
23andMers999943
23andMe allrs999943
SNP Nexus

SNPshotrs999943
SNPdbers999943
MSV3drs999943
GWAS Ctlgrs999943
GMAF0.2833
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 0.000001
Odds Ratio 1.37 [1.20-1.56]


GET Evidence
rs999943
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.262295
summary