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rs527236204

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236204(C;C)
Make rs527236204(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14935
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236204
ebirs527236204
HLIrs527236204
Exacrs527236204
Varsomers527236204
Maprs527236204
PheGenIrs527236204
hapmaprs527236204
1000 genomesrs527236204
hgdprs527236204
ensemblrs527236204
gopubmedrs527236204
geneviewrs527236204
scholarrs527236204
googlers527236204
pharmgkbrs527236204
gwascentralrs527236204
openSNPrs527236204
23andMers527236204
23andMe allrs527236204
SNP Nexus

SNPshotrs527236204
SNPdbers527236204
MSV3drs527236204
GWAS Ctlgrs527236204
Max Magnitude0
ClinVar
Risk rs527236204(C;C)
Alt rs527236204(C;C)
Reference rs527236204(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.14935T>C
CLNSRC ClinVar
CLNACC RCV000133451.1,