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rs4244274

From SNPedia

Orientationplus
Stabilizedplus
Make rs4244274(C;C)
Make rs4244274(C;T)
Make rs4244274(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position108675280
is asnp
is mentioned by
dbSNPrs4244274
ebirs4244274
HLIrs4244274
Exacrs4244274
Varsomers4244274
Maprs4244274
PheGenIrs4244274
hapmaprs4244274
1000 genomesrs4244274
hgdprs4244274
ensemblrs4244274
gopubmedrs4244274
geneviewrs4244274
scholarrs4244274
googlers4244274
pharmgkbrs4244274
gwascentralrs4244274
openSNPrs4244274
23andMers4244274
23andMe allrs4244274
SNP Nexus

SNPshotrs4244274
SNPdbers4244274
MSV3drs4244274
GWAS Ctlgrs4244274
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 4E-9
Odds Ratio NR NR