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rs10916814

From SNPedia

Orientationplus
Stabilizedplus
Make rs10916814(C;C)
Make rs10916814(C;T)
Make rs10916814(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position20566438
is asnp
is mentioned by
dbSNPrs10916814
ebirs10916814
HLIrs10916814
Exacrs10916814
Varsomers10916814
Maprs10916814
PheGenIrs10916814
hapmaprs10916814
1000 genomesrs10916814
hgdprs10916814
ensemblrs10916814
gopubmedrs10916814
geneviewrs10916814
scholarrs10916814
googlers10916814
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openSNPrs10916814
23andMers10916814
23andMe allrs10916814
SNP Nexus

SNPshotrs10916814
SNPdbers10916814
MSV3drs10916814
GWAS Ctlgrs10916814
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 5E-10
Odds Ratio NR NR