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rs207460002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs207460002(A;G)
Make rs207460002(G;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15579
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207460002
ebirs207460002
HLIrs207460002
Exacrs207460002
Varsomers207460002
Maprs207460002
PheGenIrs207460002
hapmaprs207460002
1000 genomesrs207460002
hgdprs207460002
ensemblrs207460002
gopubmedrs207460002
geneviewrs207460002
scholarrs207460002
googlers207460002
pharmgkbrs207460002
gwascentralrs207460002
openSNPrs207460002
23andMers207460002
23andMe allrs207460002
SNP Nexus

SNPshotrs207460002
SNPdbers207460002
MSV3drs207460002
GWAS Ctlgrs207460002
Max Magnitude0
ClinVar
Risk rs207460002(G;G)
Alt rs207460002(G;G)
Reference rs207460002(A;A)
Significance Pathogenic
Disease Multisystem disorder
Variation info
Gene CYTB
CLNDBN Multisystem disorder
Reversed 0
HGVS NC_012920.1:m.15579A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010321.2,