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rs527236162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236162(C;T)
Make rs527236162(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14753
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236162
ebirs527236162
HLIrs527236162
Exacrs527236162
Varsomers527236162
Maprs527236162
PheGenIrs527236162
hapmaprs527236162
1000 genomesrs527236162
hgdprs527236162
ensemblrs527236162
gopubmedrs527236162
geneviewrs527236162
scholarrs527236162
googlers527236162
pharmgkbrs527236162
gwascentralrs527236162
openSNPrs527236162
23andMers527236162
23andMe allrs527236162
SNP Nexus

SNPshotrs527236162
SNPdbers527236162
MSV3drs527236162
GWAS Ctlgrs527236162
Max Magnitude0
ClinVar
Risk rs527236162(T;T)
Alt rs527236162(T;T)
Reference rs527236162(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.14753C>T
CLNSRC ClinVar
CLNACC RCV000133404.1,