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rs527236207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236207(C;T)
Make rs527236207(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15259
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236207
ebirs527236207
HLIrs527236207
Exacrs527236207
Varsomers527236207
Maprs527236207
PheGenIrs527236207
hapmaprs527236207
1000 genomesrs527236207
hgdprs527236207
ensemblrs527236207
gopubmedrs527236207
geneviewrs527236207
scholarrs527236207
googlers527236207
pharmgkbrs527236207
gwascentralrs527236207
openSNPrs527236207
23andMers527236207
23andMe allrs527236207
SNP Nexus

SNPshotrs527236207
SNPdbers527236207
MSV3drs527236207
GWAS Ctlgrs527236207
Max Magnitude0
ClinVar
Risk rs527236207(T;T)
Alt rs527236207(T;T)
Reference rs527236207(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15259C>T
CLNSRC ClinVar
CLNACC RCV000133454.1,