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

rs527236044

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236044(C;C)
Make rs527236044(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15287
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236044
ebirs527236044
HLIrs527236044
Exacrs527236044
Varsomers527236044
Maprs527236044
PheGenIrs527236044
hapmaprs527236044
1000 genomesrs527236044
hgdprs527236044
ensemblrs527236044
gopubmedrs527236044
geneviewrs527236044
scholarrs527236044
googlers527236044
pharmgkbrs527236044
gwascentralrs527236044
openSNPrs527236044
23andMers527236044
23andMe allrs527236044
SNP Nexus

SNPshotrs527236044
SNPdbers527236044
MSV3drs527236044
GWAS Ctlgrs527236044
Max Magnitude0
ClinVar
Risk rs527236044(C;C)
Alt rs527236044(C;C)
Reference rs527236044(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.15287T>C
CLNSRC ClinVar
CLNACC RCV000128805.1,