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rs527236211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236211(C;C)
Make rs527236211(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15670
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236211
ebirs527236211
HLIrs527236211
Exacrs527236211
Varsomers527236211
Maprs527236211
PheGenIrs527236211
hapmaprs527236211
1000 genomesrs527236211
hgdprs527236211
ensemblrs527236211
gopubmedrs527236211
geneviewrs527236211
scholarrs527236211
googlers527236211
pharmgkbrs527236211
gwascentralrs527236211
openSNPrs527236211
23andMers527236211
23andMe allrs527236211
SNP Nexus

SNPshotrs527236211
SNPdbers527236211
MSV3drs527236211
GWAS Ctlgrs527236211
Max Magnitude0
ClinVar
Risk rs527236211(C;C)
Alt rs527236211(C;C)
Reference rs527236211(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15670T>C
CLNSRC ClinVar
CLNACC RCV000133458.1,