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

rs527236183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236183(C;T)
Make rs527236183(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15385
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236183
ebirs527236183
HLIrs527236183
Exacrs527236183
Varsomers527236183
Maprs527236183
PheGenIrs527236183
hapmaprs527236183
1000 genomesrs527236183
hgdprs527236183
ensemblrs527236183
gopubmedrs527236183
geneviewrs527236183
scholarrs527236183
googlers527236183
pharmgkbrs527236183
gwascentralrs527236183
openSNPrs527236183
23andMers527236183
23andMe allrs527236183
SNP Nexus

SNPshotrs527236183
SNPdbers527236183
MSV3drs527236183
GWAS Ctlgrs527236183
Max Magnitude0
ClinVar
Risk rs527236183(T;T)
Alt rs527236183(T;T)
Reference Rs527236183(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.15385C>T
CLNSRC ClinVar
CLNACC RCV000133427.1,