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rs13068223

From SNPedia

Orientationplus
Stabilizedplus
Make rs13068223(A;A)
Make rs13068223(A;G)
Make rs13068223(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position156753166
GeneLINC00886
is asnp
is mentioned by
dbSNPrs13068223
ebirs13068223
HLIrs13068223
Exacrs13068223
Varsomers13068223
Maprs13068223
PheGenIrs13068223
hapmaprs13068223
1000 genomesrs13068223
hgdprs13068223
ensemblrs13068223
gopubmedrs13068223
geneviewrs13068223
scholarrs13068223
googlers13068223
pharmgkbrs13068223
gwascentralrs13068223
openSNPrs13068223
23andMers13068223
23andMe allrs13068223
SNP Nexus

SNPshotrs13068223
SNPdbers13068223
MSV3drs13068223
GWAS Ctlgrs13068223
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 5E-9
Odds Ratio NR NR