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rs16864714

From SNPedia

Orientationplus
Stabilizedplus
Make rs16864714(C;C)
Make rs16864714(C;T)
Make rs16864714(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position152926122
is asnp
is mentioned by
dbSNPrs16864714
ebirs16864714
HLIrs16864714
Exacrs16864714
Varsomers16864714
Maprs16864714
PheGenIrs16864714
hapmaprs16864714
1000 genomesrs16864714
hgdprs16864714
ensemblrs16864714
gopubmedrs16864714
geneviewrs16864714
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openSNPrs16864714
23andMers16864714
23andMe allrs16864714
SNP Nexus

SNPshotrs16864714
SNPdbers16864714
MSV3drs16864714
GWAS Ctlgrs16864714
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