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rs4601326

From SNPedia

Orientationplus
Stabilizedplus
Make rs4601326(A;A)
Make rs4601326(A;G)
Make rs4601326(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position130479982
is asnp
is mentioned by
dbSNPrs4601326
ebirs4601326
HLIrs4601326
Exacrs4601326
Varsomers4601326
Maprs4601326
PheGenIrs4601326
hapmaprs4601326
1000 genomesrs4601326
hgdprs4601326
ensemblrs4601326
gopubmedrs4601326
geneviewrs4601326
scholarrs4601326
googlers4601326
pharmgkbrs4601326
gwascentralrs4601326
openSNPrs4601326
23andMers4601326
23andMe allrs4601326
SNP Nexus

SNPshotrs4601326
SNPdbers4601326
MSV3drs4601326
GWAS Ctlgrs4601326
GMAF0.2796
Max Magnitude
? (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.