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rs397507296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar
Make rs397507296(C;T)
Make rs397507296(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32337273
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507296
ClinGenrs397507296
ebirs397507296
HLIrs397507296
Exacrs397507296
Varsomers397507296
Maprs397507296
PheGenIrs397507296
hapmaprs397507296
1000 genomesrs397507296
hgdprs397507296
ensemblrs397507296
gopubmedrs397507296
geneviewrs397507296
scholarrs397507296
googlers397507296
pharmgkbrs397507296
gwascentralrs397507296
openSNPrs397507296
23andMers397507296
23andMe allrs397507296
SNP Nexus

SNPshotrs397507296
SNPdbers397507296
MSV3drs397507296
GWAS Ctlgrs397507296
Max Magnitude6
ClinVar
Risk rs397507296(A;A) rs397507296(T;T)
Alt rs397507296(A;A) rs397507296(T;T)
Reference Rs397507296(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer not specified Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not specified Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911410C>A; NC_000013.10:g.32911410C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129596.3, RCV000241198.1, RCV000031388.4, RCV000165120.2, RCV000220429.1, RCV000471898.1,