Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507410

From SNPedia

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


Make rs397507410(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376717
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507410
dbSNP (old)rs397507410
ClinGenrs397507410
ebirs397507410
HLIrs397507410
Exacrs397507410
Gnomadrs397507410
Varsomers397507410
Maprs397507410
PheGenIrs397507410
Biobankrs397507410
1000 genomesrs397507410
hgdprs397507410
ensemblrs397507410
gopubmedrs397507410
geneviewrs397507410
scholarrs397507410
googlers397507410
pharmgkbrs397507410
gwascentralrs397507410
openSNPrs397507410
23andMers397507410
23andMe allrs397507410
SNP Nexus

SNPshotrs397507410
SNPdbers397507410
MSV3drs397507410
GWAS Ctlgrs397507410
Max Magnitude6
ClinVar
Risk rs397507410(-;-)
Alt rs397507410(-;-)
Reference Rs397507410(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32950854delC
CLNSRC ClinVar
CLNACC RCV000031761.5, RCV000219473.1, RCV000476800.1,