Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606617(A;G)
Make rs267606617(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position1555
GeneBIRC6
is asnp
is mentioned by
dbSNPrs267606617
ebirs267606617
HLIrs267606617
Exacrs267606617
Varsomers267606617
Maprs267606617
PheGenIrs267606617
hapmaprs267606617
1000 genomesrs267606617
hgdprs267606617
ensemblrs267606617
gopubmedrs267606617
geneviewrs267606617
scholarrs267606617
googlers267606617
pharmgkbrs267606617
gwascentralrs267606617
openSNPrs267606617
23andMers267606617
23andMe allrs267606617
SNP Nexus

SNPshotrs267606617
SNPdbers267606617
MSV3drs267606617
GWAS Ctlgrs267606617
Max Magnitude0
ClinVar
Risk rs267606617(G;G)
Alt rs267606617(G;G)
Reference rs267606617(A;A)
Significance Drug-response
Disease Aminoglycoside-induced deafness Deafness Cardiomyopathy aminoglycoside antibacterials response - Toxicity/ADR not provided
Variation info
Gene
CLNDBN Aminoglycoside-induced deafness Deafness, nonsyndromic sensorineural, mitochondrial Cardiomyopathy, restrictive aminoglycoside antibacterials response - Toxicity/ADR not provided
Reversed 0
HGVS NC_012920.1:m.1555A>G
CLNSRC OMIM Allelic Variant PharmGKB
CLNACC RCV000010254.5, RCV000010255.6, RCV000010256.5, RCV000211153.1, RCV000224935.1,