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rs527236199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236199(G;G)
Make rs527236199(G;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15932
is asnp
is mentioned by
dbSNPrs527236199
ebirs527236199
HLIrs527236199
Exacrs527236199
Varsomers527236199
Maprs527236199
PheGenIrs527236199
hapmaprs527236199
1000 genomesrs527236199
hgdprs527236199
ensemblrs527236199
gopubmedrs527236199
geneviewrs527236199
scholarrs527236199
googlers527236199
pharmgkbrs527236199
gwascentralrs527236199
openSNPrs527236199
23andMers527236199
23andMe allrs527236199
SNP Nexus

SNPshotrs527236199
SNPdbers527236199
MSV3drs527236199
GWAS Ctlgrs527236199
Max Magnitude0
ClinVar
Risk rs527236199(C,G;C,G)
Alt rs527236199(C,G;C,G)
Reference rs527236199(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15932T>G
CLNSRC
CLNACC RCV000133443.1,