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rs4462272

From SNPedia

Orientationplus
Stabilizedplus
Make rs4462272(C;C)
Make rs4462272(C;T)
Make rs4462272(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position100063786
GeneCPN1
is asnp
is mentioned by
dbSNPrs4462272
ebirs4462272
HLIrs4462272
Exacrs4462272
Varsomers4462272
Maprs4462272
PheGenIrs4462272
hapmaprs4462272
1000 genomesrs4462272
hgdprs4462272
ensemblrs4462272
gopubmedrs4462272
geneviewrs4462272
scholarrs4462272
googlers4462272
pharmgkbrs4462272
gwascentralrs4462272
openSNPrs4462272
23andMers4462272
23andMe allrs4462272
SNP Nexus

SNPshotrs4462272
SNPdbers4462272
MSV3drs4462272
GWAS Ctlgrs4462272
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment (interaction)
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 8E-9
Odds Ratio NR NR