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rs527236042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236042(C;C)
Make rs527236042(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14783
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236042
ebirs527236042
HLIrs527236042
Exacrs527236042
Varsomers527236042
Maprs527236042
PheGenIrs527236042
hapmaprs527236042
1000 genomesrs527236042
hgdprs527236042
ensemblrs527236042
gopubmedrs527236042
geneviewrs527236042
scholarrs527236042
googlers527236042
pharmgkbrs527236042
gwascentralrs527236042
openSNPrs527236042
23andMers527236042
23andMe allrs527236042
SNP Nexus

SNPshotrs527236042
SNPdbers527236042
MSV3drs527236042
GWAS Ctlgrs527236042
Merged fromRs28357680
Max Magnitude0
ClinVar
Risk rs527236042(C;C)
Alt rs527236042(C;C)
Reference rs527236042(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.14783T>C
CLNSRC ClinVar
CLNACC RCV000128803.1,