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rs397507702

From SNPedia

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


Make rs397507702(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338376
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507702
dbSNP (old)rs397507702
ClinGenrs397507702
ebirs397507702
HLIrs397507702
Exacrs397507702
Gnomadrs397507702
Varsomers397507702
Maprs397507702
PheGenIrs397507702
Biobankrs397507702
1000 genomesrs397507702
hgdprs397507702
ensemblrs397507702
gopubmedrs397507702
geneviewrs397507702
scholarrs397507702
googlers397507702
pharmgkbrs397507702
gwascentralrs397507702
openSNPrs397507702
23andMers397507702
23andMe allrs397507702
SNP Nexus

SNPshotrs397507702
SNPdbers397507702
MSV3drs397507702
GWAS Ctlgrs397507702
Max Magnitude6
ClinVar
Risk rs397507702(-;-)
Alt rs397507702(-;-)
Reference Rs397507702(T;T)
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.32912513delT
CLNSRC ClinVar
CLNACC RCV000044332.2, RCV000257014.2,