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rs527236200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236200(C;C)
Make rs527236200(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15943
is asnp
is mentioned by
dbSNPrs527236200
ebirs527236200
HLIrs527236200
Exacrs527236200
Varsomers527236200
Maprs527236200
PheGenIrs527236200
hapmaprs527236200
1000 genomesrs527236200
hgdprs527236200
ensemblrs527236200
gopubmedrs527236200
geneviewrs527236200
scholarrs527236200
googlers527236200
pharmgkbrs527236200
gwascentralrs527236200
openSNPrs527236200
23andMers527236200
23andMe allrs527236200
SNP Nexus

SNPshotrs527236200
SNPdbers527236200
MSV3drs527236200
GWAS Ctlgrs527236200
Max Magnitude0
ClinVar
Risk rs527236200(C;C)
Alt rs527236200(C;C)
Reference rs527236200(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15943T>C
CLNSRC
CLNACC RCV000133444.1,