Have questions? Visit https://www.reddit.com/r/SNPedia

rs528808

From SNPedia

Orientationminus
Stabilizedminus
Make rs528808(C;C)
Make rs528808(C;T)
Make rs528808(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position99656413
is asnp
is mentioned by
dbSNPrs528808
dbSNP (old)rs528808
ClinGenrs528808
ebirs528808
HLIrs528808
Exacrs528808
Gnomadrs528808
Varsomers528808
Maprs528808
PheGenIrs528808
Biobankrs528808
1000 genomesrs528808
hgdprs528808
ensemblrs528808
gopubmedrs528808
geneviewrs528808
scholarrs528808
googlers528808
pharmgkbrs528808
gwascentralrs528808
openSNPrs528808
23andMers528808
23andMe allrs528808
SNP Nexus

SNPshotrs528808
SNPdbers528808
MSV3drs528808
GWAS Ctlgrs528808
Max Magnitude
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 6E-6
Odds Ratio .12 [NR] unit increase