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rs397508013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397508013(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379389
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508013
ClinGenrs397508013
ebirs397508013
HLIrs397508013
Exacrs397508013
Varsomers397508013
Maprs397508013
PheGenIrs397508013
Biobankrs397508013
1000 genomesrs397508013
hgdprs397508013
ensemblrs397508013
gopubmedrs397508013
geneviewrs397508013
scholarrs397508013
googlers397508013
pharmgkbrs397508013
gwascentralrs397508013
openSNPrs397508013
23andMers397508013
23andMe allrs397508013
SNP Nexus

SNPshotrs397508013
SNPdbers397508013
MSV3drs397508013
GWAS Ctlgrs397508013
Max Magnitude6
ClinVar
Risk rs397508013(G;G)
Alt rs397508013(G;G)
Reference Rs397508013(-;-)
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.32953526_32953527insG
CLNSRC ClinVar
CLNACC RCV000045637.2, RCV000257304.1,