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rs4512366

From SNPedia

Orientationplus
Stabilizedplus
Make rs4512366(A;A)
Make rs4512366(A;G)
Make rs4512366(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position124447478
is asnp
is mentioned by
dbSNPrs4512366
dbSNP (classic)rs4512366
ClinGenrs4512366
ebirs4512366
HLIrs4512366
Exacrs4512366
Gnomadrs4512366
Varsomers4512366
LitVarrs4512366
Maprs4512366
PheGenIrs4512366
Biobankrs4512366
1000 genomesrs4512366
hgdprs4512366
ensemblrs4512366
geneviewrs4512366
scholarrs4512366
googlers4512366
pharmgkbrs4512366
gwascentralrs4512366
openSNPrs4512366
23andMers4512366
SNPshotrs4512366
SNPdbers4512366
MSV3drs4512366
GWAS Ctlgrs4512366
GMAF0.1635
Max Magnitude0
? (A;A) (A;G) (G;G) 28


OMIM612448
DescAGE-RELATED HEARING IMPAIRMENT 1; ARHI1
Variant
Relatedalso


[PMID 18760390OA-icon.png] Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.