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rs527236195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236195(A;A)
Make rs527236195(A;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15884
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236195
ebirs527236195
HLIrs527236195
Exacrs527236195
Varsomers527236195
Maprs527236195
PheGenIrs527236195
hapmaprs527236195
1000 genomesrs527236195
hgdprs527236195
ensemblrs527236195
gopubmedrs527236195
geneviewrs527236195
scholarrs527236195
googlers527236195
pharmgkbrs527236195
gwascentralrs527236195
openSNPrs527236195
23andMers527236195
23andMe allrs527236195
SNP Nexus

SNPshotrs527236195
SNPdbers527236195
MSV3drs527236195
GWAS Ctlgrs527236195
Merged fromRs28617642
Max Magnitude0
ClinVar
Risk rs527236195(A,C;A,C)
Alt rs527236195(A,C;A,C)
Reference rs527236195(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of ovary not specified
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary not specified
Reversed 0
HGVS NC_012920.1:m.15884G>A; NC_012920.1:m.15884G>C
CLNSRC ClinVar
CLNACC RCV000133439.1, RCV000238892.1,