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rs527236191

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236191(A;G)
Make rs527236191(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15649
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236191
ebirs527236191
HLIrs527236191
Exacrs527236191
Varsomers527236191
Maprs527236191
PheGenIrs527236191
hapmaprs527236191
1000 genomesrs527236191
hgdprs527236191
ensemblrs527236191
gopubmedrs527236191
geneviewrs527236191
scholarrs527236191
googlers527236191
pharmgkbrs527236191
gwascentralrs527236191
openSNPrs527236191
23andMers527236191
23andMe allrs527236191
SNP Nexus

SNPshotrs527236191
SNPdbers527236191
MSV3drs527236191
GWAS Ctlgrs527236191
Max Magnitude0
ClinVar
Risk rs527236191(G;G)
Alt rs527236191(G;G)
Reference rs527236191(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15649A>G
CLNSRC ClinVar
CLNACC RCV000133435.1,