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rs8003722

From SNPedia

Orientationplus
Stabilizedplus
Make rs8003722(A;A)
Make rs8003722(A;G)
Make rs8003722(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position68851545
is asnp
is mentioned by
dbSNPrs8003722
ebirs8003722
HLIrs8003722
Exacrs8003722
Varsomers8003722
Maprs8003722
PheGenIrs8003722
hapmaprs8003722
1000 genomesrs8003722
hgdprs8003722
ensemblrs8003722
gopubmedrs8003722
geneviewrs8003722
scholarrs8003722
googlers8003722
pharmgkbrs8003722
gwascentralrs8003722
openSNPrs8003722
23andMers8003722
23andMe allrs8003722
SNP Nexus

SNPshotrs8003722
SNPdbers8003722
MSV3drs8003722
GWAS Ctlgrs8003722
Max Magnitude
? (A;A) (A;G) (G;G) 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 8E-9
Odds Ratio NR NR