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rs267606619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606619(C;T)
Make rs267606619(T;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position1494
GeneBIRC6
is asnp
is mentioned by
dbSNPrs267606619
ebirs267606619
HLIrs267606619
Exacrs267606619
Varsomers267606619
Maprs267606619
PheGenIrs267606619
hapmaprs267606619
1000 genomesrs267606619
hgdprs267606619
ensemblrs267606619
gopubmedrs267606619
geneviewrs267606619
scholarrs267606619
googlers267606619
pharmgkbrs267606619
gwascentralrs267606619
openSNPrs267606619
23andMers267606619
23andMe allrs267606619
SNP Nexus

SNPshotrs267606619
SNPdbers267606619
MSV3drs267606619
GWAS Ctlgrs267606619
Max Magnitude0
ClinVar
Risk rs267606619(T;T)
Alt rs267606619(T;T)
Reference rs267606619(C;C)
Significance Drug-response
Disease Aminoglycoside-induced deafness Deafness aminoglycoside antibacterials response - Toxicity/ADR
Variation info
Gene
CLNDBN Aminoglycoside-induced deafness Deafness, nonsyndromic sensorineural, mitochondrial aminoglycoside antibacterials response - Toxicity/ADR
Reversed 0
HGVS NC_012920.1:m.1494C>T
CLNSRC OMIM Allelic Variant PharmGKB
CLNACC RCV000010262.3, RCV000010263.3, RCV000211324.1,