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rs527236202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236202(A;G)
Make rs527236202(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14732
is asnp
is mentioned by
dbSNPrs527236202
ebirs527236202
HLIrs527236202
Exacrs527236202
Varsomers527236202
Maprs527236202
PheGenIrs527236202
hapmaprs527236202
1000 genomesrs527236202
hgdprs527236202
ensemblrs527236202
gopubmedrs527236202
geneviewrs527236202
scholarrs527236202
googlers527236202
pharmgkbrs527236202
gwascentralrs527236202
openSNPrs527236202
23andMers527236202
23andMe allrs527236202
SNP Nexus

SNPshotrs527236202
SNPdbers527236202
MSV3drs527236202
GWAS Ctlgrs527236202
Max Magnitude0
ClinVar
Risk rs527236202(G;G)
Alt rs527236202(G;G)
Reference rs527236202(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.14732A>G
CLNSRC
CLNACC RCV000133449.1,