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rs527236188

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236188(C;C)
Make rs527236188(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15511
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236188
dbSNP (classic)rs527236188
ClinGenrs527236188
ebirs527236188
HLIrs527236188
Exacrs527236188
Gnomadrs527236188
Varsomers527236188
LitVarrs527236188
Maprs527236188
PheGenIrs527236188
Biobankrs527236188
1000 genomesrs527236188
hgdprs527236188
ensemblrs527236188
geneviewrs527236188
scholarrs527236188
googlers527236188
pharmgkbrs527236188
gwascentralrs527236188
openSNPrs527236188
23andMers527236188
SNPshotrs527236188
SNPdbers527236188
MSV3drs527236188
GWAS Ctlgrs527236188
Max Magnitude0
ClinVar
Risk rs527236188(C;C)
Alt rs527236188(C;C)
Reference Rs527236188(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of ovary not provided
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary not provided
Reversed 0
HGVS NC_012920.1:m.15511T>C
CLNSRC ClinVar
CLNACC RCV000133432.1, RCV000223961.1,