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rs587777133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777133(C;T)
Make rs587777133(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position21722977
GeneOTOA
is asnp
is mentioned by
dbSNPrs587777133
ebirs587777133
HLIrs587777133
Exacrs587777133
Varsomers587777133
Maprs587777133
PheGenIrs587777133
hapmaprs587777133
1000 genomesrs587777133
hgdprs587777133
ensemblrs587777133
gopubmedrs587777133
geneviewrs587777133
scholarrs587777133
googlers587777133
pharmgkbrs587777133
gwascentralrs587777133
openSNPrs587777133
23andMers587777133
23andMe allrs587777133
SNP Nexus

SNPshotrs587777133
SNPdbers587777133
MSV3drs587777133
GWAS Ctlgrs587777133
Max Magnitude0
ClinVar
Risk rs587777133(T;T)
Alt rs587777133(T;T)
Reference rs587777133(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOA
CLNDBN Deafness, autosomal recessive 22
Reversed 0
HGVS NC_000016.9:g.21734298C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087055.3,