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rs878853223

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853223(-;-)
Make rs878853223(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position133462338
GeneEYA4
is asnp
is mentioned by
dbSNPrs878853223
ebirs878853223
HLIrs878853223
Exacrs878853223
Varsomers878853223
Maprs878853223
PheGenIrs878853223
hapmaprs878853223
1000 genomesrs878853223
hgdprs878853223
ensemblrs878853223
gopubmedrs878853223
geneviewrs878853223
scholarrs878853223
googlers878853223
pharmgkbrs878853223
gwascentralrs878853223
openSNPrs878853223
23andMers878853223
23andMe allrs878853223
SNP Nexus

SNPshotrs878853223
SNPdbers878853223
MSV3drs878853223
GWAS Ctlgrs878853223
Max Magnitude0
ClinVar
Risk rs878853223(;)
Alt rs878853223(;)
Reference rs878853223(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene EYA4 LOC101928164
CLNDBN Deafness, autosomal dominant 10
Reversed 0
HGVS NC_000006.11:g.133783476delC
CLNSRC
CLNACC RCV000225045.1,