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rs527236182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236182(A;G)
Make rs527236182(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15363
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236182
ebirs527236182
HLIrs527236182
Exacrs527236182
Varsomers527236182
Maprs527236182
PheGenIrs527236182
hapmaprs527236182
1000 genomesrs527236182
hgdprs527236182
ensemblrs527236182
gopubmedrs527236182
geneviewrs527236182
scholarrs527236182
googlers527236182
pharmgkbrs527236182
gwascentralrs527236182
openSNPrs527236182
23andMers527236182
23andMe allrs527236182
SNP Nexus

SNPshotrs527236182
SNPdbers527236182
MSV3drs527236182
GWAS Ctlgrs527236182
Max Magnitude0
ClinVar
Risk rs527236182(G;G)
Alt rs527236182(G;G)
Reference rs527236182(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15363A>G
CLNSRC ClinVar
CLNACC RCV000133426.1,