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rs527236187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236187(C;C)
Make rs527236187(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15470
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236187
ebirs527236187
HLIrs527236187
Exacrs527236187
Varsomers527236187
Maprs527236187
PheGenIrs527236187
hapmaprs527236187
1000 genomesrs527236187
hgdprs527236187
ensemblrs527236187
gopubmedrs527236187
geneviewrs527236187
scholarrs527236187
googlers527236187
pharmgkbrs527236187
gwascentralrs527236187
openSNPrs527236187
23andMers527236187
23andMe allrs527236187
SNP Nexus

SNPshotrs527236187
SNPdbers527236187
MSV3drs527236187
GWAS Ctlgrs527236187
Max Magnitude0
ClinVar
Risk rs527236187(C;C)
Alt rs527236187(C;C)
Reference rs527236187(T;T)
Significance Probable-Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene CYTB
CLNDBN Familial cancer of breast not provided
Reversed 0
HGVS NC_012920.1:m.15470T>C
CLNSRC ClinVar
CLNACC RCV000133431.1, RCV000224601.1,