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rs527236177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236177(A;A)
Make rs527236177(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15323
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236177
dbSNP (old)rs527236177
ClinGenrs527236177
ebirs527236177
HLIrs527236177
Exacrs527236177
Gnomadrs527236177
Varsomers527236177
Maprs527236177
PheGenIrs527236177
Biobankrs527236177
1000 genomesrs527236177
hgdprs527236177
ensemblrs527236177
gopubmedrs527236177
geneviewrs527236177
scholarrs527236177
googlers527236177
pharmgkbrs527236177
gwascentralrs527236177
openSNPrs527236177
23andMers527236177
23andMe allrs527236177
SNP Nexus

SNPshotrs527236177
SNPdbers527236177
MSV3drs527236177
GWAS Ctlgrs527236177
Max Magnitude0
ClinVar
Risk rs527236177(A;A)
Alt rs527236177(A;A)
Reference Rs527236177(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.15323G>A
CLNSRC ClinVar
CLNACC RCV000133419.1,