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rs397507642

From SNPedia

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


Make rs397507642(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337141
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507642
dbSNP (old)rs397507642
ClinGenrs397507642
ebirs397507642
HLIrs397507642
Exacrs397507642
Gnomadrs397507642
Varsomers397507642
Maprs397507642
PheGenIrs397507642
Biobankrs397507642
1000 genomesrs397507642
hgdprs397507642
ensemblrs397507642
gopubmedrs397507642
geneviewrs397507642
scholarrs397507642
googlers397507642
pharmgkbrs397507642
gwascentralrs397507642
openSNPrs397507642
23andMers397507642
23andMe allrs397507642
SNP Nexus

SNPshotrs397507642
SNPdbers397507642
MSV3drs397507642
GWAS Ctlgrs397507642
Max Magnitude6
ClinVar
Risk rs397507642(-;-)
Alt rs397507642(-;-)
Reference Rs397507642(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.32911278delT
CLNSRC ClinVar
CLNACC RCV000044056.2, RCV000256522.2,