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rs28358569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28358569(A;G)
Make rs28358569(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position827
is asnp
is mentioned by
dbSNPrs28358569
ebirs28358569
HLIrs28358569
Exacrs28358569
Varsomers28358569
Maprs28358569
PheGenIrs28358569
hapmaprs28358569
1000 genomesrs28358569
hgdprs28358569
ensemblrs28358569
gopubmedrs28358569
geneviewrs28358569
scholarrs28358569
googlers28358569
pharmgkbrs28358569
gwascentralrs28358569
openSNPrs28358569
23andMers28358569
23andMe allrs28358569
SNP Nexus

SNPshotrs28358569
SNPdbers28358569
MSV3drs28358569
GWAS Ctlgrs28358569
Merged fromRs386508207
Max Magnitude0
ClinVar
Risk rs28358569(G;G)
Alt rs28358569(G;G)
Reference rs28358569(A;A)
Significance Pathogenic
Disease Deafness Aminoglycoside-induced deafness
Variation info
Gene
CLNDBN Deafness, nonsyndromic sensorineural, mitochondrial Aminoglycoside-induced deafness
Reversed 0
HGVS NC_012920.1:m.827A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010265.2, RCV000010266.2,