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rs527236171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236171(C;T)
Make rs527236171(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15058
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236171
ebirs527236171
HLIrs527236171
Exacrs527236171
Varsomers527236171
Maprs527236171
PheGenIrs527236171
hapmaprs527236171
1000 genomesrs527236171
hgdprs527236171
ensemblrs527236171
gopubmedrs527236171
geneviewrs527236171
scholarrs527236171
googlers527236171
pharmgkbrs527236171
gwascentralrs527236171
openSNPrs527236171
23andMers527236171
23andMe allrs527236171
SNP Nexus

SNPshotrs527236171
SNPdbers527236171
MSV3drs527236171
GWAS Ctlgrs527236171
Max Magnitude0
ClinVar
Risk rs527236171(T;T)
Alt rs527236171(T;T)
Reference rs527236171(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15058C>T
CLNSRC ClinVar
CLNACC RCV000133413.1,