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rs527236164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236164(C;T)
Make rs527236164(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14800
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236164
ebirs527236164
HLIrs527236164
Exacrs527236164
Varsomers527236164
Maprs527236164
PheGenIrs527236164
hapmaprs527236164
1000 genomesrs527236164
hgdprs527236164
ensemblrs527236164
gopubmedrs527236164
geneviewrs527236164
scholarrs527236164
googlers527236164
pharmgkbrs527236164
gwascentralrs527236164
openSNPrs527236164
23andMers527236164
23andMe allrs527236164
SNP Nexus

SNPshotrs527236164
SNPdbers527236164
MSV3drs527236164
GWAS Ctlgrs527236164
Max Magnitude0
ClinVar
Risk rs527236164(T;T)
Alt rs527236164(T;T)
Reference rs527236164(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.14800C>T
CLNSRC ClinVar
CLNACC RCV000133406.1,