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rs527236198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236198(A;A)
Make rs527236198(A;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15928
is asnp
is mentioned by
dbSNPrs527236198
ebirs527236198
HLIrs527236198
Exacrs527236198
Varsomers527236198
Maprs527236198
PheGenIrs527236198
hapmaprs527236198
1000 genomesrs527236198
hgdprs527236198
ensemblrs527236198
gopubmedrs527236198
geneviewrs527236198
scholarrs527236198
googlers527236198
pharmgkbrs527236198
gwascentralrs527236198
openSNPrs527236198
23andMers527236198
23andMe allrs527236198
SNP Nexus

SNPshotrs527236198
SNPdbers527236198
MSV3drs527236198
GWAS Ctlgrs527236198
Max Magnitude0
ClinVar
Risk rs527236198(A;A)
Alt rs527236198(A;A)
Reference rs527236198(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15928G>A
CLNSRC
CLNACC RCV000133442.1,