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rs4674973

From SNPedia

Orientationplus
Stabilizedplus
Make rs4674973(A;A)
Make rs4674973(A;C)
Make rs4674973(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position225154561
is asnp
is mentioned by
dbSNPrs4674973
ebirs4674973
HLIrs4674973
Exacrs4674973
Varsomers4674973
Maprs4674973
PheGenIrs4674973
hapmaprs4674973
1000 genomesrs4674973
hgdprs4674973
ensemblrs4674973
gopubmedrs4674973
geneviewrs4674973
scholarrs4674973
googlers4674973
pharmgkbrs4674973
gwascentralrs4674973
openSNPrs4674973
23andMers4674973
23andMe allrs4674973
SNP Nexus

SNPshotrs4674973
SNPdbers4674973
MSV3drs4674973
GWAS Ctlgrs4674973
Max Magnitude
GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 4E-6
Odds Ratio .04 [NR] unit increase