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rs2281636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2281636(G;G)
Make rs2281636(G;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position99732646
GeneCOX15, CUTC
is asnp
is mentioned by
dbSNPrs2281636
dbSNP (old)rs2281636
ClinGenrs2281636
ebirs2281636
HLIrs2281636
Exacrs2281636
Gnomadrs2281636
Varsomers2281636
Maprs2281636
PheGenIrs2281636
Biobankrs2281636
1000 genomesrs2281636
hgdprs2281636
ensemblrs2281636
gopubmedrs2281636
geneviewrs2281636
scholarrs2281636
googlers2281636
pharmgkbrs2281636
gwascentralrs2281636
openSNPrs2281636
23andMers2281636
23andMe allrs2281636
SNP Nexus

SNPshotrs2281636
SNPdbers2281636
MSV3drs2281636
GWAS Ctlgrs2281636
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 6E-6
Odds Ratio .03 [NR] mg/dL increase


ClinVar
Risk rs2281636(G;G)
Alt rs2281636(G;G)
Reference Rs2281636(T;T)
Significance Probable-non-pathogenic
Disease Cytochrome-c oxidase deficiency
Variation info
Gene CUTC COX15
CLNDBN Cytochrome-c oxidase deficiency
Reversed 0
HGVS NC_000010.10:g.101492403T>G
CLNSRC
CLNACC RCV000383808.1,