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rs397507900

From SNPedia

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


Make rs397507900(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355036
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507900
dbSNP (old)rs397507900
ClinGenrs397507900
ebirs397507900
HLIrs397507900
Exacrs397507900
Gnomadrs397507900
Varsomers397507900
Maprs397507900
PheGenIrs397507900
Biobankrs397507900
1000 genomesrs397507900
hgdprs397507900
ensemblrs397507900
gopubmedrs397507900
geneviewrs397507900
scholarrs397507900
googlers397507900
pharmgkbrs397507900
gwascentralrs397507900
openSNPrs397507900
23andMers397507900
23andMe allrs397507900
SNP Nexus

SNPshotrs397507900
SNPdbers397507900
MSV3drs397507900
GWAS Ctlgrs397507900
Max Magnitude6
ClinVar
Risk rs397507900(-;-)
Alt rs397507900(-;-)
Reference Rs397507900(C;C)
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.32929173delC
CLNSRC ClinVar
CLNACC RCV000045158.2, RCV000256985.2,