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rs397507670

From SNPedia

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


Make rs397507670(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337808
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507670
dbSNP (old)rs397507670
ClinGenrs397507670
ebirs397507670
HLIrs397507670
Exacrs397507670
Gnomadrs397507670
Varsomers397507670
Maprs397507670
PheGenIrs397507670
Biobankrs397507670
1000 genomesrs397507670
hgdprs397507670
ensemblrs397507670
gopubmedrs397507670
geneviewrs397507670
scholarrs397507670
googlers397507670
pharmgkbrs397507670
gwascentralrs397507670
openSNPrs397507670
23andMers397507670
23andMe allrs397507670
SNP Nexus

SNPshotrs397507670
SNPdbers397507670
MSV3drs397507670
GWAS Ctlgrs397507670
Max Magnitude6
ClinVar
Risk rs397507670(-;-)
Alt rs397507670(-;-)
Reference Rs397507670(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.32911945delC
CLNSRC ClinVar
CLNACC RCV000044200.2, RCV000240972.2,