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rs207460005

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATT;AATT) 0 common in clinvar
(TTAA;TTAA) 0 common in clinvar
Make rs207460005(-;-)
Make rs207460005(-;TTAA)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14787
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207460005
ebirs207460005
HLIrs207460005
Exacrs207460005
Varsomers207460005
Maprs207460005
PheGenIrs207460005
hapmaprs207460005
1000 genomesrs207460005
hgdprs207460005
ensemblrs207460005
gopubmedrs207460005
geneviewrs207460005
scholarrs207460005
googlers207460005
pharmgkbrs207460005
gwascentralrs207460005
openSNPrs207460005
23andMers207460005
23andMe allrs207460005
SNP Nexus

SNPshotrs207460005
SNPdbers207460005
MSV3drs207460005
GWAS Ctlgrs207460005
Max Magnitude0
ClinVar
Risk rs207460005(;)
Alt rs207460005(;)
Reference rs207460005(AATT;AATT)
Significance Pathogenic
Disease Parkinsonism/MELAS overlap syndrome
Variation info
Gene CYTB
CLNDBN Parkinsonism/MELAS overlap syndrome
Reversed 0
HGVS NC_012920.1:m.14787_14790delTTAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010324.2,