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rs527236166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236166(C;T)
Make rs527236166(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14950
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236166
ebirs527236166
HLIrs527236166
Exacrs527236166
Varsomers527236166
Maprs527236166
PheGenIrs527236166
hapmaprs527236166
1000 genomesrs527236166
hgdprs527236166
ensemblrs527236166
gopubmedrs527236166
geneviewrs527236166
scholarrs527236166
googlers527236166
pharmgkbrs527236166
gwascentralrs527236166
openSNPrs527236166
23andMers527236166
23andMe allrs527236166
SNP Nexus

SNPshotrs527236166
SNPdbers527236166
MSV3drs527236166
GWAS Ctlgrs527236166
Max Magnitude0
ClinVar
Risk rs527236166(T;T)
Alt rs527236166(T;T)
Reference rs527236166(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.14950C>T
CLNSRC ClinVar
CLNACC RCV000133408.1,