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rs397507373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507373(-;-)
Make rs397507373(-;A)
Make rs397507373(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340921
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507373
ebirs397507373
HLIrs397507373
Exacrs397507373
Varsomers397507373
Maprs397507373
PheGenIrs397507373
hapmaprs397507373
1000 genomesrs397507373
hgdprs397507373
ensemblrs397507373
gopubmedrs397507373
geneviewrs397507373
scholarrs397507373
googlers397507373
pharmgkbrs397507373
gwascentralrs397507373
openSNPrs397507373
23andMers397507373
23andMe allrs397507373
SNP Nexus

SNPshotrs397507373
SNPdbers397507373
MSV3drs397507373
GWAS Ctlgrs397507373
Max Magnitude0
ClinVar
Risk rs397507373(A;A)
Alt rs397507373(A;A)
Reference rs397507373(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32915058dupA
CLNSRC ClinVar
CLNACC RCV000031635.3, RCV000122925.1, RCV000160303.1, RCV000214634.1,