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rs527236196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236196(A;A)
Make rs527236196(A;C)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15890
is asnp
is mentioned by
dbSNPrs527236196
ebirs527236196
HLIrs527236196
Exacrs527236196
Varsomers527236196
Maprs527236196
PheGenIrs527236196
hapmaprs527236196
1000 genomesrs527236196
hgdprs527236196
ensemblrs527236196
gopubmedrs527236196
geneviewrs527236196
scholarrs527236196
googlers527236196
pharmgkbrs527236196
gwascentralrs527236196
openSNPrs527236196
23andMers527236196
23andMe allrs527236196
SNP Nexus

SNPshotrs527236196
SNPdbers527236196
MSV3drs527236196
GWAS Ctlgrs527236196
Max Magnitude0
ClinVar
Risk rs527236196(A;A)
Alt rs527236196(A;A)
Reference rs527236196(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15890C>A
CLNSRC
CLNACC RCV000133440.1,