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rs267606620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606620(C;C)
Make rs267606620(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position1291
GeneBIRC6
is asnp
is mentioned by
dbSNPrs267606620
ebirs267606620
HLIrs267606620
Exacrs267606620
Varsomers267606620
Maprs267606620
PheGenIrs267606620
hapmaprs267606620
1000 genomesrs267606620
hgdprs267606620
ensemblrs267606620
gopubmedrs267606620
geneviewrs267606620
scholarrs267606620
googlers267606620
pharmgkbrs267606620
gwascentralrs267606620
openSNPrs267606620
23andMers267606620
23andMe allrs267606620
SNP Nexus

SNPshotrs267606620
SNPdbers267606620
MSV3drs267606620
GWAS Ctlgrs267606620
GMAF0.001871
Max Magnitude0
ClinVar
Risk rs267606620(C;C)
Alt rs267606620(C;C)
Reference rs267606620(T;T)
Significance Pathogenic
Disease Deafness not provided
Variation info
Gene
CLNDBN Deafness, nonsyndromic sensorineural, mitochondrial not provided
Reversed 0
HGVS NC_012920.1:m.1291T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010258.2, RCV000224305.1,