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rs527236045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236045(A;A)
Make rs527236045(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15301
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236045
dbSNP (classic)rs527236045
ClinGenrs527236045
ebirs527236045
HLIrs527236045
Exacrs527236045
Gnomadrs527236045
Varsomers527236045
LitVarrs527236045
Maprs527236045
PheGenIrs527236045
Biobankrs527236045
1000 genomesrs527236045
hgdprs527236045
ensemblrs527236045
geneviewrs527236045
scholarrs527236045
googlers527236045
pharmgkbrs527236045
gwascentralrs527236045
openSNPrs527236045
23andMers527236045
SNPshotrs527236045
SNPdbers527236045
MSV3drs527236045
GWAS Ctlgrs527236045
Merged fromRs28573847
Max Magnitude0
? (A;A) (A;G) (G;G) 28


ClinVar
Risk rs527236045(A;A)
Alt rs527236045(A;A)
Reference Rs527236045(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15301G>A
CLNSRC ClinVar
CLNACC RCV000128806.1,