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rs527236173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236173(C;C)
Make rs527236173(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15214
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236173
ebirs527236173
HLIrs527236173
Exacrs527236173
Varsomers527236173
Maprs527236173
PheGenIrs527236173
hapmaprs527236173
1000 genomesrs527236173
hgdprs527236173
ensemblrs527236173
gopubmedrs527236173
geneviewrs527236173
scholarrs527236173
googlers527236173
pharmgkbrs527236173
gwascentralrs527236173
openSNPrs527236173
23andMers527236173
23andMe allrs527236173
SNP Nexus

SNPshotrs527236173
SNPdbers527236173
MSV3drs527236173
GWAS Ctlgrs527236173
Max Magnitude0
ClinVar
Risk rs527236173(C;C)
Alt rs527236173(C;C)
Reference rs527236173(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.15214T>C
CLNSRC ClinVar
CLNACC RCV000133415.1,