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rs4685724

From SNPedia

Orientationplus
Stabilizedplus
Make rs4685724(C;C)
Make rs4685724(C;T)
Make rs4685724(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position3993759
GeneSUMF1
is asnp
is mentioned by
dbSNPrs4685724
dbSNP (classic)rs4685724
ClinGenrs4685724
ebirs4685724
HLIrs4685724
Exacrs4685724
Gnomadrs4685724
Varsomers4685724
LitVarrs4685724
Maprs4685724
PheGenIrs4685724
Biobankrs4685724
1000 genomesrs4685724
hgdprs4685724
ensemblrs4685724
geneviewrs4685724
scholarrs4685724
googlers4685724
pharmgkbrs4685724
gwascentralrs4685724
openSNPrs4685724
23andMers4685724
SNPshotrs4685724
SNPdbers4685724
MSV3drs4685724
GWAS Ctlgrs4685724
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 24939585OA-icon.png]
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 1E-9
Odds Ratio NR NR