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rs12776158

From SNPedia

Orientationplus
Stabilizedplus
Make rs12776158(C;C)
Make rs12776158(C;T)
Make rs12776158(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position69458338
GeneTSPAN15
is asnp
is mentioned by
dbSNPrs12776158
ebirs12776158
HLIrs12776158
Exacrs12776158
Varsomers12776158
Maprs12776158
PheGenIrs12776158
hapmaprs12776158
1000 genomesrs12776158
hgdprs12776158
ensemblrs12776158
gopubmedrs12776158
geneviewrs12776158
scholarrs12776158
googlers12776158
pharmgkbrs12776158
gwascentralrs12776158
openSNPrs12776158
23andMers12776158
23andMe allrs12776158
SNP Nexus

SNPshotrs12776158
SNPdbers12776158
MSV3drs12776158
GWAS Ctlgrs12776158
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 6E-9
Odds Ratio NR NR