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

rs76547188

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76547188(C;T)
Make rs76547188(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position22120859
GeneHR
is asnp
is mentioned by
dbSNPrs76547188
dbSNP (old)rs76547188
ClinGenrs76547188
ebirs76547188
HLIrs76547188
Exacrs76547188
Varsomers76547188
Maprs76547188
PheGenIrs76547188
Biobankrs76547188
1000 genomesrs76547188
hgdprs76547188
ensemblrs76547188
gopubmedrs76547188
geneviewrs76547188
scholarrs76547188
googlers76547188
pharmgkbrs76547188
gwascentralrs76547188
openSNPrs76547188
23andMers76547188
23andMe allrs76547188
SNP Nexus

SNPshotrs76547188
SNPdbers76547188
MSV3drs76547188
GWAS Ctlgrs76547188
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 5E-6
Odds Ratio .03 [NR] pg/mL increase
ClinVar
Risk rs76547188(T;T)
Alt rs76547188(T;T)
Reference Rs76547188(C;C)
Significance Probable-non-pathogenic
Disease Alopecia universalis Atrichia with papular lesions
Variation info
Gene HR
CLNDBN Alopecia universalis Atrichia with papular lesions
Reversed 0
HGVS NC_000008.10:g.21978372C>T
CLNSRC
CLNACC RCV000268215.1, RCV000321099.1,