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rs207460001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs207460001(C;C)
Make rs207460001(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15197
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207460001
ebirs207460001
HLIrs207460001
Exacrs207460001
Varsomers207460001
Maprs207460001
PheGenIrs207460001
hapmaprs207460001
1000 genomesrs207460001
hgdprs207460001
ensemblrs207460001
gopubmedrs207460001
geneviewrs207460001
scholarrs207460001
googlers207460001
pharmgkbrs207460001
gwascentralrs207460001
openSNPrs207460001
23andMers207460001
23andMe allrs207460001
SNP Nexus

SNPshotrs207460001
SNPdbers207460001
MSV3drs207460001
GWAS Ctlgrs207460001
Max Magnitude0
ClinVar
Risk rs207460001(C;C)
Alt rs207460001(C;C)
Reference rs207460001(T;T)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene CYTB
CLNDBN Exercise intolerance
Reversed 0
HGVS NC_012920.1:m.15197T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010320.4,