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rs397507627

From SNPedia

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


Make rs397507627(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336797
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507627
dbSNP (old)rs397507627
ClinGenrs397507627
ebirs397507627
HLIrs397507627
Exacrs397507627
Gnomadrs397507627
Varsomers397507627
Maprs397507627
PheGenIrs397507627
Biobankrs397507627
1000 genomesrs397507627
hgdprs397507627
ensemblrs397507627
gopubmedrs397507627
geneviewrs397507627
scholarrs397507627
googlers397507627
pharmgkbrs397507627
gwascentralrs397507627
openSNPrs397507627
23andMers397507627
23andMe allrs397507627
SNP Nexus

SNPshotrs397507627
SNPdbers397507627
MSV3drs397507627
GWAS Ctlgrs397507627
Max Magnitude6
ClinVar
Risk rs397507627(-;-)
Alt rs397507627(-;-)
Reference Rs397507627(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910934delC
CLNSRC ClinVar
CLNACC RCV000043995.3, RCV000241109.1,