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rs1958581

From SNPedia

Orientationplus
Stabilizedplus
Make rs1958581(C;C)
Make rs1958581(C;G)
Make rs1958581(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position34332393
is asnp
is mentioned by
dbSNPrs1958581
dbSNP (classic)rs1958581
ClinGenrs1958581
ebirs1958581
HLIrs1958581
Exacrs1958581
Gnomadrs1958581
Varsomers1958581
LitVarrs1958581
Maprs1958581
PheGenIrs1958581
Biobankrs1958581
1000 genomesrs1958581
hgdprs1958581
ensemblrs1958581
geneviewrs1958581
scholarrs1958581
googlers1958581
pharmgkbrs1958581
gwascentralrs1958581
openSNPrs1958581
23andMers1958581
SNPshotrs1958581
SNPdbers1958581
MSV3drs1958581
GWAS Ctlgrs1958581
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 24939585OA-icon.png]
Trait Age-related hearing impairment
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 8E-6
Odds Ratio .14 [NR] unit decrease