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rs527236175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236175(C;C)
Make rs527236175(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15289
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236175
ebirs527236175
HLIrs527236175
Exacrs527236175
Varsomers527236175
Maprs527236175
PheGenIrs527236175
hapmaprs527236175
1000 genomesrs527236175
hgdprs527236175
ensemblrs527236175
gopubmedrs527236175
geneviewrs527236175
scholarrs527236175
googlers527236175
pharmgkbrs527236175
gwascentralrs527236175
openSNPrs527236175
23andMers527236175
23andMe allrs527236175
SNP Nexus

SNPshotrs527236175
SNPdbers527236175
MSV3drs527236175
GWAS Ctlgrs527236175
Max Magnitude0
ClinVar
Risk rs527236175(C;C)
Alt rs527236175(C;C)
Reference rs527236175(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.15289T>C
CLNSRC ClinVar
CLNACC RCV000133417.1,