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rs527236169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236169(C;C)
Make rs527236169(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15001
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236169
ebirs527236169
HLIrs527236169
Exacrs527236169
Varsomers527236169
Maprs527236169
PheGenIrs527236169
hapmaprs527236169
1000 genomesrs527236169
hgdprs527236169
ensemblrs527236169
gopubmedrs527236169
geneviewrs527236169
scholarrs527236169
googlers527236169
pharmgkbrs527236169
gwascentralrs527236169
openSNPrs527236169
23andMers527236169
23andMe allrs527236169
SNP Nexus

SNPshotrs527236169
SNPdbers527236169
MSV3drs527236169
GWAS Ctlgrs527236169
Max Magnitude0
ClinVar
Risk rs527236169(C;C)
Alt rs527236169(C;C)
Reference rs527236169(T;T)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15001T>C
CLNSRC ClinVar
CLNACC RCV000133411.1,