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rs527236190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236190(C;T)
Make rs527236190(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15637
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236190
ebirs527236190
HLIrs527236190
Exacrs527236190
Varsomers527236190
Maprs527236190
PheGenIrs527236190
hapmaprs527236190
1000 genomesrs527236190
hgdprs527236190
ensemblrs527236190
gopubmedrs527236190
geneviewrs527236190
scholarrs527236190
googlers527236190
pharmgkbrs527236190
gwascentralrs527236190
openSNPrs527236190
23andMers527236190
23andMe allrs527236190
SNP Nexus

SNPshotrs527236190
SNPdbers527236190
MSV3drs527236190
GWAS Ctlgrs527236190
Max Magnitude0
ClinVar
Risk rs527236190(T;T)
Alt rs527236190(T;T)
Reference rs527236190(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.15637C>T
CLNSRC ClinVar
CLNACC RCV000133434.1,