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rs207459998

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs207459998(A;A)
Make rs207459998(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position14846
GeneCYTB
is asnp
is mentioned by
dbSNPrs207459998
dbSNP (old)rs207459998
ClinGenrs207459998
ebirs207459998
HLIrs207459998
Exacrs207459998
Gnomadrs207459998
Varsomers207459998
Maprs207459998
PheGenIrs207459998
Biobankrs207459998
1000 genomesrs207459998
hgdprs207459998
ensemblrs207459998
gopubmedrs207459998
geneviewrs207459998
scholarrs207459998
googlers207459998
pharmgkbrs207459998
gwascentralrs207459998
openSNPrs207459998
23andMers207459998
23andMe allrs207459998
SNP Nexus

SNPshotrs207459998
SNPdbers207459998
MSV3drs207459998
GWAS Ctlgrs207459998
Max Magnitude0
ClinVar
Risk rs207459998(A;A)
Alt rs207459998(A;A)
Reference Rs207459998(G;G)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene CYTB
CLNDBN Exercise intolerance
Reversed 0
HGVS NC_012920.1:m.14846G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010317.2,