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rs4788099

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs4788099(A;G)
Make rs4788099(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position28844406
GeneMIR4721, TUFM
is asnp
is mentioned by
dbSNPrs4788099
dbSNP (classic)rs4788099
ClinGenrs4788099
ebirs4788099
HLIrs4788099
Exacrs4788099
Gnomadrs4788099
Varsomers4788099
LitVarrs4788099
Maprs4788099
PheGenIrs4788099
Biobankrs4788099
1000 genomesrs4788099
hgdprs4788099
ensemblrs4788099
geneviewrs4788099
scholarrs4788099
googlers4788099
pharmgkbrs4788099
gwascentralrs4788099
openSNPrs4788099
23andMers4788099
SNPshotrs4788099
SNPdbers4788099
MSV3drs4788099
GWAS Ctlgrs4788099
GMAF0.2658
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23001569OA-icon.png] Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals


[PMID 22513296OA-icon.png] Obesity susceptibility loci and dietary intake in the Look AHEAD Trial.


ClinVar
Risk rs4788099(G;G)
Alt rs4788099(G;G)
Reference Rs4788099(A;A)
Significance Non-pathogenic
Disease Combined oxidative phosphorylation deficiency
Variation info
Gene TUFM NPIPB8 MIR4721
CLNDBN Combined oxidative phosphorylation deficiency
Reversed 0
HGVS NC_000016.9:g.28855727A>G
CLNSRC
CLNACC RCV000265919.1,