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rs397507920

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar


Make rs397507920(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356536
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507920
dbSNP (old)rs397507920
ClinGenrs397507920
ebirs397507920
HLIrs397507920
Exacrs397507920
Varsomers397507920
Maprs397507920
PheGenIrs397507920
Biobankrs397507920
1000 genomesrs397507920
hgdprs397507920
ensemblrs397507920
gopubmedrs397507920
geneviewrs397507920
scholarrs397507920
googlers397507920
pharmgkbrs397507920
gwascentralrs397507920
openSNPrs397507920
23andMers397507920
23andMe allrs397507920
SNP Nexus

SNPshotrs397507920
SNPdbers397507920
MSV3drs397507920
GWAS Ctlgrs397507920
Max Magnitude6
ClinVar
Risk rs397507920(-;-)
Alt rs397507920(-;-)
Reference Rs397507920(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32930673delC
CLNSRC ClinVar
CLNACC RCV000045243.2, RCV000241012.1,