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rs207459997

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs207459997(A;A)
Make rs207459997(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15615
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207459997
ebirs207459997
HLIrs207459997
Exacrs207459997
Varsomers207459997
Maprs207459997
PheGenIrs207459997
hapmaprs207459997
1000 genomesrs207459997
hgdprs207459997
ensemblrs207459997
gopubmedrs207459997
geneviewrs207459997
scholarrs207459997
googlers207459997
pharmgkbrs207459997
gwascentralrs207459997
openSNPrs207459997
23andMers207459997
23andMe allrs207459997
SNP Nexus

SNPshotrs207459997
SNPdbers207459997
MSV3drs207459997
GWAS Ctlgrs207459997
Max Magnitude0
ClinVar
Risk rs207459997(A;A)
Alt rs207459997(A;A)
Reference rs207459997(G;G)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene CYTB
CLNDBN Exercise intolerance
Reversed 0
HGVS NC_012920.1:m.15615G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010316.4,