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rs397507716

From SNPedia

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


Make rs397507716(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326113
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507716
dbSNP (old)rs397507716
ClinGenrs397507716
ebirs397507716
HLIrs397507716
Exacrs397507716
Gnomadrs397507716
Varsomers397507716
Maprs397507716
PheGenIrs397507716
Biobankrs397507716
1000 genomesrs397507716
hgdprs397507716
ensemblrs397507716
gopubmedrs397507716
geneviewrs397507716
scholarrs397507716
googlers397507716
pharmgkbrs397507716
gwascentralrs397507716
openSNPrs397507716
23andMers397507716
23andMe allrs397507716
SNP Nexus

SNPshotrs397507716
SNPdbers397507716
MSV3drs397507716
GWAS Ctlgrs397507716
Max Magnitude6
ClinVar
Risk rs397507716(-;-)
Alt rs397507716(-;-)
Reference Rs397507716(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.32900250delA
CLNSRC ClinVar
CLNACC RCV000044403.2, RCV000257290.2,