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rs1869026

From SNPedia

Orientationminus
Stabilizedminus
Make rs1869026(G;G)
Make rs1869026(G;T)
Make rs1869026(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position120583705
is asnp
is mentioned by
dbSNPrs1869026
ebirs1869026
HLIrs1869026
Exacrs1869026
Varsomers1869026
Maprs1869026
PheGenIrs1869026
hapmaprs1869026
1000 genomesrs1869026
hgdprs1869026
ensemblrs1869026
gopubmedrs1869026
geneviewrs1869026
scholarrs1869026
googlers1869026
pharmgkbrs1869026
gwascentralrs1869026
openSNPrs1869026
23andMers1869026
23andMe allrs1869026
SNP Nexus

SNPshotrs1869026
SNPdbers1869026
MSV3drs1869026
GWAS Ctlgrs1869026
Max Magnitude
? (G;G) (G;T) (T;T) 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 4E-10
Odds Ratio NR NR