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rs397507773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507773(-;-)
Make rs397507773(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339562
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507773
ebirs397507773
HLIrs397507773
Exacrs397507773
Varsomers397507773
Maprs397507773
PheGenIrs397507773
hapmaprs397507773
1000 genomesrs397507773
hgdprs397507773
ensemblrs397507773
gopubmedrs397507773
geneviewrs397507773
scholarrs397507773
googlers397507773
pharmgkbrs397507773
gwascentralrs397507773
openSNPrs397507773
23andMers397507773
23andMe allrs397507773
SNP Nexus

SNPshotrs397507773
SNPdbers397507773
MSV3drs397507773
GWAS Ctlgrs397507773
Max Magnitude0
ClinVar
Risk rs397507773(;)
Alt rs397507773(;)
Reference rs397507773(AA;AA)
Significance 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.32913699_32913700delAA
CLNSRC ClinVar
CLNACC RCV000044606.2, RCV000219814.1,