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rs2309322

From SNPedia

Orientationplus
Stabilizedplus
Make rs2309322(C;C)
Make rs2309322(C;T)
Make rs2309322(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position180318981
is asnp
is mentioned by
dbSNPrs2309322
ebirs2309322
HLIrs2309322
Exacrs2309322
Varsomers2309322
Maprs2309322
PheGenIrs2309322
hapmaprs2309322
1000 genomesrs2309322
hgdprs2309322
ensemblrs2309322
gopubmedrs2309322
geneviewrs2309322
scholarrs2309322
googlers2309322
pharmgkbrs2309322
gwascentralrs2309322
openSNPrs2309322
23andMers2309322
23andMe allrs2309322
SNP Nexus

SNPshotrs2309322
SNPdbers2309322
MSV3drs2309322
GWAS Ctlgrs2309322
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 1E-9
Odds Ratio NR NR