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rs527236193

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236193(A;G)
Make rs527236193(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15758
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236193
ebirs527236193
HLIrs527236193
Exacrs527236193
Varsomers527236193
Maprs527236193
PheGenIrs527236193
hapmaprs527236193
1000 genomesrs527236193
hgdprs527236193
ensemblrs527236193
gopubmedrs527236193
geneviewrs527236193
scholarrs527236193
googlers527236193
pharmgkbrs527236193
gwascentralrs527236193
openSNPrs527236193
23andMers527236193
23andMe allrs527236193
SNP Nexus

SNPshotrs527236193
SNPdbers527236193
MSV3drs527236193
GWAS Ctlgrs527236193
Max Magnitude0
ClinVar
Risk rs527236193(G;G)
Alt rs527236193(G;G)
Reference rs527236193(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.15758A>G
CLNSRC ClinVar
CLNACC RCV000133437.1,