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rs397507452

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507452(A;G)
Make rs397507452(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position7443
GeneMT-CO1
is asnp
is mentioned by
dbSNPrs397507452
ebirs397507452
HLIrs397507452
Exacrs397507452
Varsomers397507452
Maprs397507452
PheGenIrs397507452
hapmaprs397507452
1000 genomesrs397507452
hgdprs397507452
ensemblrs397507452
gopubmedrs397507452
geneviewrs397507452
scholarrs397507452
googlers397507452
pharmgkbrs397507452
gwascentralrs397507452
openSNPrs397507452
23andMers397507452
23andMe allrs397507452
SNP Nexus

SNPshotrs397507452
SNPdbers397507452
MSV3drs397507452
GWAS Ctlgrs397507452
Max Magnitude0
ClinVar
Risk rs397507452(G;G)
Alt rs397507452(G;G)
Reference rs397507452(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene COX1
CLNDBN Deafness, nonsyndromic sensorineural, mitochondrial
Reversed 0
HGVS NC_012920.1:m.7443A>G
CLNSRC
CLNACC RCV000202557.1,