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rs527236186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236186(C;T)
Make rs527236186(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15459
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236186
ebirs527236186
HLIrs527236186
Exacrs527236186
Varsomers527236186
Maprs527236186
PheGenIrs527236186
hapmaprs527236186
1000 genomesrs527236186
hgdprs527236186
ensemblrs527236186
gopubmedrs527236186
geneviewrs527236186
scholarrs527236186
googlers527236186
pharmgkbrs527236186
gwascentralrs527236186
openSNPrs527236186
23andMers527236186
23andMe allrs527236186
SNP Nexus

SNPshotrs527236186
SNPdbers527236186
MSV3drs527236186
GWAS Ctlgrs527236186
Max Magnitude0
ClinVar
Risk rs527236186(T;T)
Alt rs527236186(T;T)
Reference rs527236186(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15459C>T
CLNSRC ClinVar
CLNACC RCV000133430.1,