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rs527236163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236163(C;C)
Make rs527236163(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14784
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236163
ebirs527236163
HLIrs527236163
Exacrs527236163
Varsomers527236163
Maprs527236163
PheGenIrs527236163
hapmaprs527236163
1000 genomesrs527236163
hgdprs527236163
ensemblrs527236163
gopubmedrs527236163
geneviewrs527236163
scholarrs527236163
googlers527236163
pharmgkbrs527236163
gwascentralrs527236163
openSNPrs527236163
23andMers527236163
23andMe allrs527236163
SNP Nexus

SNPshotrs527236163
SNPdbers527236163
MSV3drs527236163
GWAS Ctlgrs527236163
Max Magnitude0
ClinVar
Risk rs527236163(C;C)
Alt rs527236163(C;C)
Reference rs527236163(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.14784T>C
CLNSRC ClinVar
CLNACC RCV000133405.1,