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rs267606618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606618(C;C)
Make rs267606618(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position1095
GeneBIRC6
is asnp
is mentioned by
dbSNPrs267606618
ebirs267606618
HLIrs267606618
Exacrs267606618
Varsomers267606618
Maprs267606618
PheGenIrs267606618
hapmaprs267606618
1000 genomesrs267606618
hgdprs267606618
ensemblrs267606618
gopubmedrs267606618
geneviewrs267606618
scholarrs267606618
googlers267606618
pharmgkbrs267606618
gwascentralrs267606618
openSNPrs267606618
23andMers267606618
23andMe allrs267606618
SNP Nexus

SNPshotrs267606618
SNPdbers267606618
MSV3drs267606618
GWAS Ctlgrs267606618
GMAF0.0009355
Max Magnitude0
ClinVar
Risk rs267606618(C;C)
Alt rs267606618(C;C)
Reference rs267606618(T;T)
Significance Drug-response
Disease Aminoglycoside-induced deafness Deafness Auditory neuropathy not specified aminoglycoside antibacterials response - Toxicity/ADR
Variation info
Gene
CLNDBN Aminoglycoside-induced deafness Deafness, nonsyndromic sensorineural, mitochondrial Auditory neuropathy not specified aminoglycoside antibacterials response - Toxicity/ADR
Reversed 0
HGVS NC_012920.1:m.1095T>C
CLNSRC OMIM Allelic Variant PharmGKB
CLNACC RCV000010259.2, RCV000010260.2, RCV000010261.2, RCV000035031.2, RCV000211239.1,