Have questions? Visit https://www.reddit.com/r/SNPedia

rs527236185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236185(C;C)
Make rs527236185(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15458
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236185
ebirs527236185
HLIrs527236185
Exacrs527236185
Varsomers527236185
Maprs527236185
PheGenIrs527236185
hapmaprs527236185
1000 genomesrs527236185
hgdprs527236185
ensemblrs527236185
gopubmedrs527236185
geneviewrs527236185
scholarrs527236185
googlers527236185
pharmgkbrs527236185
gwascentralrs527236185
openSNPrs527236185
23andMers527236185
23andMe allrs527236185
SNP Nexus

SNPshotrs527236185
SNPdbers527236185
MSV3drs527236185
GWAS Ctlgrs527236185
Max Magnitude0
ClinVar
Risk rs527236185(C;C)
Alt rs527236185(C;C)
Reference rs527236185(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.15458T>C
CLNSRC ClinVar
CLNACC RCV000133429.1,