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rs397507678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507678(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337996
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507678
dbSNP (old)rs397507678
ClinGenrs397507678
ebirs397507678
HLIrs397507678
Exacrs397507678
Gnomadrs397507678
Varsomers397507678
Maprs397507678
PheGenIrs397507678
Biobankrs397507678
1000 genomesrs397507678
hgdprs397507678
ensemblrs397507678
gopubmedrs397507678
geneviewrs397507678
scholarrs397507678
googlers397507678
pharmgkbrs397507678
gwascentralrs397507678
openSNPrs397507678
23andMers397507678
23andMe allrs397507678
SNP Nexus

SNPshotrs397507678
SNPdbers397507678
MSV3drs397507678
GWAS Ctlgrs397507678
Max Magnitude6
ClinVar
Risk rs397507678(T;T)
Alt rs397507678(T;T)
Reference Rs397507678(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32912133dupT
CLNSRC ClinVar
CLNACC RCV000044234.2, RCV000257562.2, RCV000483680.1,