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rs10769908

From SNPedia

Orientationplus
Stabilizedplus
Make rs10769908(C;C)
Make rs10769908(C;T)
Make rs10769908(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position8462542
GeneSTK33
is asnp
is mentioned by
dbSNPrs10769908
ebirs10769908
HLIrs10769908
Exacrs10769908
Varsomers10769908
Maprs10769908
PheGenIrs10769908
hapmaprs10769908
1000 genomesrs10769908
hgdprs10769908
ensemblrs10769908
gopubmedrs10769908
geneviewrs10769908
scholarrs10769908
googlers10769908
pharmgkbrs10769908
gwascentralrs10769908
openSNPrs10769908
23andMers10769908
23andMe allrs10769908
SNP Nexus

SNPshotrs10769908
SNPdbers10769908
MSV3drs10769908
GWAS Ctlgrs10769908
GMAF0.4435
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19079261OA-icon.png]
Trait Body mass index
Title Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Risk Allele C
P-val 0.000001
Odds Ratio NR NR


[PMID 19553259OA-icon.png] Common body mass index-associated variants confer risk of extreme obesity.

[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs10769908
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.52381
summary