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rs724159989

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs724159989(C;C)
Make rs724159989(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position7505
is asnp
is mentioned by
dbSNPrs724159989
ebirs724159989
HLIrs724159989
Exacrs724159989
Varsomers724159989
Maprs724159989
PheGenIrs724159989
hapmaprs724159989
1000 genomesrs724159989
hgdprs724159989
ensemblrs724159989
gopubmedrs724159989
geneviewrs724159989
scholarrs724159989
googlers724159989
pharmgkbrs724159989
gwascentralrs724159989
openSNPrs724159989
23andMers724159989
23andMe allrs724159989
SNP Nexus

SNPshotrs724159989
SNPdbers724159989
MSV3drs724159989
GWAS Ctlgrs724159989
Max Magnitude0
ClinVar
Risk rs724159989(C;C)
Alt rs724159989(C;C)
Reference rs724159989(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene
CLNDBN Deafness, nonsyndromic sensorineural, mitochondrial
Reversed 0
HGVS NC_012920.1:m.7505T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000033857.3,