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rs527236165

From SNPedia

Merged intors386419981
Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236165(C;G)
Make rs527236165(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14891
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236165
ebirs527236165
HLIrs527236165
Exacrs527236165
Varsomers527236165
Maprs527236165
PheGenIrs527236165
hapmaprs527236165
1000 genomesrs527236165
hgdprs527236165
ensemblrs527236165
gopubmedrs527236165
geneviewrs527236165
scholarrs527236165
googlers527236165
pharmgkbrs527236165
gwascentralrs527236165
openSNPrs527236165
23andMers527236165
23andMe allrs527236165
SNP Nexus

SNPshotrs527236165
SNPdbers527236165
MSV3drs527236165
GWAS Ctlgrs527236165
StatusMerged into rs386419981
Max Magnitude0
ClinVar
Risk rs527236165(G;G)
Alt rs527236165(G;G)
Reference rs527236165(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.14891C>G
CLNSRC ClinVar
CLNACC RCV000133407.1,