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rs397507592

From SNPedia

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


Make rs397507592(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332992
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507592
dbSNP (old)rs397507592
ClinGenrs397507592
ebirs397507592
HLIrs397507592
Exacrs397507592
Gnomadrs397507592
Varsomers397507592
Maprs397507592
PheGenIrs397507592
Biobankrs397507592
1000 genomesrs397507592
hgdprs397507592
ensemblrs397507592
gopubmedrs397507592
geneviewrs397507592
scholarrs397507592
googlers397507592
pharmgkbrs397507592
gwascentralrs397507592
openSNPrs397507592
23andMers397507592
23andMe allrs397507592
SNP Nexus

SNPshotrs397507592
SNPdbers397507592
MSV3drs397507592
GWAS Ctlgrs397507592
Max Magnitude6
ClinVar
Risk rs397507592(-;-)
Alt rs397507592(-;-)
Reference Rs397507592(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.32907129delT
CLNSRC ClinVar
CLNACC RCV000043821.2, RCV000257416.2,