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rs9329289

From SNPedia

Orientationplus
Stabilizedplus
Make rs9329289(A;A)
Make rs9329289(A;G)
Make rs9329289(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position2500197
is asnp
is mentioned by
dbSNPrs9329289
ebirs9329289
HLIrs9329289
Exacrs9329289
Varsomers9329289
Maprs9329289
PheGenIrs9329289
hapmaprs9329289
1000 genomesrs9329289
hgdprs9329289
ensemblrs9329289
gopubmedrs9329289
geneviewrs9329289
scholarrs9329289
googlers9329289
pharmgkbrs9329289
gwascentralrs9329289
openSNPrs9329289
23andMers9329289
23andMe allrs9329289
SNP Nexus

SNPshotrs9329289
SNPdbers9329289
MSV3drs9329289
GWAS Ctlgrs9329289
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 6E-6
Odds Ratio .10 [NR] unit increase