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rs527236189

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236189(A;A)
Make rs527236189(A;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15553
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236189
ebirs527236189
HLIrs527236189
Exacrs527236189
Varsomers527236189
Maprs527236189
PheGenIrs527236189
hapmaprs527236189
1000 genomesrs527236189
hgdprs527236189
ensemblrs527236189
gopubmedrs527236189
geneviewrs527236189
scholarrs527236189
googlers527236189
pharmgkbrs527236189
gwascentralrs527236189
openSNPrs527236189
23andMers527236189
23andMe allrs527236189
SNP Nexus

SNPshotrs527236189
SNPdbers527236189
MSV3drs527236189
GWAS Ctlgrs527236189
Max Magnitude0
ClinVar
Risk rs527236189(A;A)
Alt rs527236189(A;A)
Reference rs527236189(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.15553G>A
CLNSRC ClinVar
CLNACC RCV000133433.1,