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rs527236206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236206(A;A)
Make rs527236206(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15148
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236206
dbSNP (classic)rs527236206
ClinGenrs527236206
ebirs527236206
HLIrs527236206
Exacrs527236206
Gnomadrs527236206
Varsomers527236206
LitVarrs527236206
Maprs527236206
PheGenIrs527236206
Biobankrs527236206
1000 genomesrs527236206
hgdprs527236206
ensemblrs527236206
geneviewrs527236206
scholarrs527236206
googlers527236206
pharmgkbrs527236206
gwascentralrs527236206
openSNPrs527236206
23andMers527236206
SNPshotrs527236206
SNPdbers527236206
MSV3drs527236206
GWAS Ctlgrs527236206
Max Magnitude0
ClinVar
Risk rs527236206(A;A)
Alt rs527236206(A;A)
Reference Rs527236206(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15148G>A
CLNSRC ClinVar
CLNACC RCV000133453.1,