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rs527236179

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236179(C;T)
Make rs527236179(T;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15334
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236179
ebirs527236179
HLIrs527236179
Exacrs527236179
Varsomers527236179
Maprs527236179
PheGenIrs527236179
hapmaprs527236179
1000 genomesrs527236179
hgdprs527236179
ensemblrs527236179
gopubmedrs527236179
geneviewrs527236179
scholarrs527236179
googlers527236179
pharmgkbrs527236179
gwascentralrs527236179
openSNPrs527236179
23andMers527236179
23andMe allrs527236179
SNP Nexus

SNPshotrs527236179
SNPdbers527236179
MSV3drs527236179
GWAS Ctlgrs527236179
Max Magnitude0
ClinVar
Risk rs527236179(T;T)
Alt rs527236179(T;T)
Reference rs527236179(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15334C>T
CLNSRC ClinVar
CLNACC RCV000133421.1,