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rs527236170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236170(C;T)
Make rs527236170(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15049
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236170
ebirs527236170
HLIrs527236170
Exacrs527236170
Varsomers527236170
Maprs527236170
PheGenIrs527236170
hapmaprs527236170
1000 genomesrs527236170
hgdprs527236170
ensemblrs527236170
gopubmedrs527236170
geneviewrs527236170
scholarrs527236170
googlers527236170
pharmgkbrs527236170
gwascentralrs527236170
openSNPrs527236170
23andMers527236170
23andMe allrs527236170
SNP Nexus

SNPshotrs527236170
SNPdbers527236170
MSV3drs527236170
GWAS Ctlgrs527236170
Max Magnitude0
ClinVar
Risk rs527236170(T;T)
Alt rs527236170(T;T)
Reference rs527236170(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.15049C>T
CLNSRC ClinVar
CLNACC RCV000133412.1,