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rs397507849

From SNPedia

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


Make rs397507849(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340748
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507849
dbSNP (old)rs397507849
ClinGenrs397507849
ebirs397507849
HLIrs397507849
Exacrs397507849
Varsomers397507849
Maprs397507849
PheGenIrs397507849
Biobankrs397507849
1000 genomesrs397507849
hgdprs397507849
ensemblrs397507849
gopubmedrs397507849
geneviewrs397507849
scholarrs397507849
googlers397507849
pharmgkbrs397507849
gwascentralrs397507849
openSNPrs397507849
23andMers397507849
23andMe allrs397507849
SNP Nexus

SNPshotrs397507849
SNPdbers397507849
MSV3drs397507849
GWAS Ctlgrs397507849
Max Magnitude6
ClinVar
Risk rs397507849(-;-)
Alt rs397507849(-;-)
Reference Rs397507849(AATT;AATT)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32914885_32914888delATTA
CLNSRC ClinVar
CLNACC RCV000044930.2, RCV000166186.1, RCV000211011.2, RCV000478975.1,