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rs527236194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236194(C;C)
Make rs527236194(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15784
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236194
ebirs527236194
HLIrs527236194
Exacrs527236194
Varsomers527236194
Maprs527236194
PheGenIrs527236194
hapmaprs527236194
1000 genomesrs527236194
hgdprs527236194
ensemblrs527236194
gopubmedrs527236194
geneviewrs527236194
scholarrs527236194
googlers527236194
pharmgkbrs527236194
gwascentralrs527236194
openSNPrs527236194
23andMers527236194
23andMe allrs527236194
SNP Nexus

SNPshotrs527236194
SNPdbers527236194
MSV3drs527236194
GWAS Ctlgrs527236194
Max Magnitude0
ClinVar
Risk rs527236194(C;C)
Alt rs527236194(C;C)
Reference rs527236194(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.15784T>C
CLNSRC ClinVar
CLNACC RCV000133438.1,