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rs79509430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79509430(C;T)
Make rs79509430(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position114478626
GeneWHRN
is asnp
is mentioned by
dbSNPrs79509430
dbSNP (classic)rs79509430
ClinGenrs79509430
ebirs79509430
HLIrs79509430
Exacrs79509430
Gnomadrs79509430
Varsomers79509430
LitVarrs79509430
Maprs79509430
PheGenIrs79509430
Biobankrs79509430
1000 genomesrs79509430
hgdprs79509430
ensemblrs79509430
geneviewrs79509430
scholarrs79509430
googlers79509430
pharmgkbrs79509430
gwascentralrs79509430
openSNPrs79509430
23andMers79509430
SNPshotrs79509430
SNPdbers79509430
MSV3drs79509430
GWAS Ctlgrs79509430
Max Magnitude0
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 2E-8
Odds Ratio .06 [NR] pg/mL increase
ClinVar
Risk rs79509430(T;T)
Alt rs79509430(T;T)
Reference Rs79509430(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene WHRN DFNB31
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.117240906C>T
CLNSRC ClinVar
CLNACC RCV000038901.2,