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rs207460003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs207460003(A;A)
Make rs207460003(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15498
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207460003
ebirs207460003
HLIrs207460003
Exacrs207460003
Varsomers207460003
Maprs207460003
PheGenIrs207460003
hapmaprs207460003
1000 genomesrs207460003
hgdprs207460003
ensemblrs207460003
gopubmedrs207460003
geneviewrs207460003
scholarrs207460003
googlers207460003
pharmgkbrs207460003
gwascentralrs207460003
openSNPrs207460003
23andMers207460003
23andMe allrs207460003
SNP Nexus

SNPshotrs207460003
SNPdbers207460003
MSV3drs207460003
GWAS Ctlgrs207460003
Max Magnitude0
ClinVar
Risk rs207460003(A;A)
Alt rs207460003(A;A)
Reference rs207460003(G;G)
Significance Pathogenic
Disease Infantile histiocytoid cardiomyopathy
Variation info
Gene CYTB
CLNDBN Infantile histiocytoid cardiomyopathy
Reversed 0
HGVS NC_012920.1:m.15498G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010322.2,