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rs527236201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236201(A;A)
Make rs527236201(A;C)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15349
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236201
ebirs527236201
HLIrs527236201
Exacrs527236201
Varsomers527236201
Maprs527236201
PheGenIrs527236201
hapmaprs527236201
1000 genomesrs527236201
hgdprs527236201
ensemblrs527236201
gopubmedrs527236201
geneviewrs527236201
scholarrs527236201
googlers527236201
pharmgkbrs527236201
gwascentralrs527236201
openSNPrs527236201
23andMers527236201
23andMe allrs527236201
SNP Nexus

SNPshotrs527236201
SNPdbers527236201
MSV3drs527236201
GWAS Ctlgrs527236201
Max Magnitude0
ClinVar
Risk rs527236201(A,T;A,T)
Alt rs527236201(A,T;A,T)
Reference rs527236201(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15349C>A; NC_012920.1:m.15349C>T
CLNSRC ClinVar
CLNACC RCV000133423.1, RCV000133424.1,