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rs397507991

From SNPedia

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


Make rs397507991(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371014
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507991
dbSNP (old)rs397507991
ClinGenrs397507991
ebirs397507991
HLIrs397507991
Exacrs397507991
Gnomadrs397507991
Varsomers397507991
Maprs397507991
PheGenIrs397507991
Biobankrs397507991
1000 genomesrs397507991
hgdprs397507991
ensemblrs397507991
gopubmedrs397507991
geneviewrs397507991
scholarrs397507991
googlers397507991
pharmgkbrs397507991
gwascentralrs397507991
openSNPrs397507991
23andMers397507991
23andMe allrs397507991
SNP Nexus

SNPshotrs397507991
SNPdbers397507991
MSV3drs397507991
GWAS Ctlgrs397507991
Max Magnitude6
ClinVar
Risk rs397507991(-;-)
Alt rs397507991(-;-)
Reference Rs397507991(A;A)
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.32945151delA
CLNSRC ClinVar
CLNACC RCV000045553.2, RCV000256678.2,