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rs397507713

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507713(G;T)
Make rs397507713(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325184
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507713
ebirs397507713
HLIrs397507713
Exacrs397507713
Varsomers397507713
Maprs397507713
PheGenIrs397507713
hapmaprs397507713
1000 genomesrs397507713
hgdprs397507713
ensemblrs397507713
gopubmedrs397507713
geneviewrs397507713
scholarrs397507713
googlers397507713
pharmgkbrs397507713
gwascentralrs397507713
openSNPrs397507713
23andMers397507713
23andMe allrs397507713
SNP Nexus

SNPshotrs397507713
SNPdbers397507713
MSV3drs397507713
GWAS Ctlgrs397507713
Max Magnitude0
ClinVar
Risk rs397507713(A,T;A,T)
Alt rs397507713(A,T;A,T)
Reference rs397507713(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32899321G>T
CLNSRC ClinVar
CLNACC RCV000044379.2, RCV000213168.1,