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rs527236167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236167(C;C)
Make rs527236167(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14968
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236167
ebirs527236167
HLIrs527236167
Exacrs527236167
Varsomers527236167
Maprs527236167
PheGenIrs527236167
hapmaprs527236167
1000 genomesrs527236167
hgdprs527236167
ensemblrs527236167
gopubmedrs527236167
geneviewrs527236167
scholarrs527236167
googlers527236167
pharmgkbrs527236167
gwascentralrs527236167
openSNPrs527236167
23andMers527236167
23andMe allrs527236167
SNP Nexus

SNPshotrs527236167
SNPdbers527236167
MSV3drs527236167
GWAS Ctlgrs527236167
Max Magnitude0
ClinVar
Risk rs527236167(C;C)
Alt rs527236167(C;C)
Reference rs527236167(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.14968T>C
CLNSRC ClinVar
CLNACC RCV000133409.1,