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rs397507988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507988(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370533
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507988
dbSNP (old)rs397507988
ClinGenrs397507988
ebirs397507988
HLIrs397507988
Exacrs397507988
Gnomadrs397507988
Varsomers397507988
Maprs397507988
PheGenIrs397507988
Biobankrs397507988
1000 genomesrs397507988
hgdprs397507988
ensemblrs397507988
gopubmedrs397507988
geneviewrs397507988
scholarrs397507988
googlers397507988
pharmgkbrs397507988
gwascentralrs397507988
openSNPrs397507988
23andMers397507988
23andMe allrs397507988
SNP Nexus

SNPshotrs397507988
SNPdbers397507988
MSV3drs397507988
GWAS Ctlgrs397507988
Max Magnitude6
ClinVar
Risk rs397507988(T;T)
Alt rs397507988(T;T)
Reference Rs397507988(-;-)
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.32944670dupT
CLNSRC ClinVar
CLNACC RCV000045527.2, RCV000241216.2,