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rs4667193

From SNPedia

Orientationplus
Stabilizedplus
Make rs4667193(C;C)
Make rs4667193(C;T)
Make rs4667193(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position187761487
is asnp
is mentioned by
dbSNPrs4667193
ebirs4667193
HLIrs4667193
Exacrs4667193
Varsomers4667193
Maprs4667193
PheGenIrs4667193
hapmaprs4667193
1000 genomesrs4667193
hgdprs4667193
ensemblrs4667193
gopubmedrs4667193
geneviewrs4667193
scholarrs4667193
googlers4667193
pharmgkbrs4667193
gwascentralrs4667193
openSNPrs4667193
23andMers4667193
23andMe allrs4667193
SNP Nexus

SNPshotrs4667193
SNPdbers4667193
MSV3drs4667193
GWAS Ctlgrs4667193
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 2E-9
Odds Ratio NR NR