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rs527236041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236041(C;T)
Make rs527236041(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14766
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236041
ebirs527236041
HLIrs527236041
Exacrs527236041
Varsomers527236041
Maprs527236041
PheGenIrs527236041
hapmaprs527236041
1000 genomesrs527236041
hgdprs527236041
ensemblrs527236041
gopubmedrs527236041
geneviewrs527236041
scholarrs527236041
googlers527236041
pharmgkbrs527236041
gwascentralrs527236041
openSNPrs527236041
23andMers527236041
23andMe allrs527236041
SNP Nexus

SNPshotrs527236041
SNPdbers527236041
MSV3drs527236041
GWAS Ctlgrs527236041
Max Magnitude0
ClinVar
Risk rs527236041(T;T)
Alt rs527236041(T;T)
Reference rs527236041(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.14766C>T
CLNSRC ClinVar
CLNACC RCV000128802.1,