Have questions? Visit https://www.reddit.com/r/SNPedia

rs877674

From SNPedia

Orientationminus
Stabilizedminus
Make rs877674(C;C)
Make rs877674(C;T)
Make rs877674(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position31776605
is asnp
is mentioned by
dbSNPrs877674
ebirs877674
HLIrs877674
Exacrs877674
Varsomers877674
Maprs877674
PheGenIrs877674
hapmaprs877674
1000 genomesrs877674
hgdprs877674
ensemblrs877674
gopubmedrs877674
geneviewrs877674
scholarrs877674
googlers877674
pharmgkbrs877674
gwascentralrs877674
openSNPrs877674
23andMers877674
23andMe allrs877674
SNP Nexus

SNPshotrs877674
SNPdbers877674
MSV3drs877674
GWAS Ctlgrs877674
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 4E-11
Odds Ratio NR NR