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rs527236205

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236205(A;G)
Make rs527236205(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15061
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236205
dbSNP (classic)rs527236205
ClinGenrs527236205
ebirs527236205
HLIrs527236205
Exacrs527236205
Gnomadrs527236205
Varsomers527236205
LitVarrs527236205
Maprs527236205
PheGenIrs527236205
Biobankrs527236205
1000 genomesrs527236205
hgdprs527236205
ensemblrs527236205
geneviewrs527236205
scholarrs527236205
googlers527236205
pharmgkbrs527236205
gwascentralrs527236205
openSNPrs527236205
23andMers527236205
SNPshotrs527236205
SNPdbers527236205
MSV3drs527236205
GWAS Ctlgrs527236205
Max Magnitude0
ClinVar
Risk rs527236205(G;G)
Alt rs527236205(G;G)
Reference Rs527236205(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15061A>G
CLNSRC ClinVar
CLNACC RCV000133452.1,