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rs207460004

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs207460004(C;C)
Make rs207460004(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14849
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207460004
ebirs207460004
HLIrs207460004
Exacrs207460004
Varsomers207460004
Maprs207460004
PheGenIrs207460004
hapmaprs207460004
1000 genomesrs207460004
hgdprs207460004
ensemblrs207460004
gopubmedrs207460004
geneviewrs207460004
scholarrs207460004
googlers207460004
pharmgkbrs207460004
gwascentralrs207460004
openSNPrs207460004
23andMers207460004
23andMe allrs207460004
SNP Nexus

SNPshotrs207460004
SNPdbers207460004
MSV3drs207460004
GWAS Ctlgrs207460004
Max Magnitude0
ClinVar
Risk rs207460004(C;C)
Alt rs207460004(C;C)
Reference rs207460004(T;T)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene CYTB
CLNDBN Exercise intolerance, cardiomyopathy, and septooptic dysplasia
Reversed 0
HGVS NC_012920.1:m.14849T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010323.4,