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rs397507751

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
(CA;CA) 0 common in clinvar
Make rs397507751(-;-)
Make rs397507751(-;CA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339295
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507751
ebirs397507751
HLIrs397507751
Exacrs397507751
Varsomers397507751
Maprs397507751
PheGenIrs397507751
hapmaprs397507751
1000 genomesrs397507751
hgdprs397507751
ensemblrs397507751
gopubmedrs397507751
geneviewrs397507751
scholarrs397507751
googlers397507751
pharmgkbrs397507751
gwascentralrs397507751
openSNPrs397507751
23andMers397507751
23andMe allrs397507751
SNP Nexus

SNPshotrs397507751
SNPdbers397507751
MSV3drs397507751
GWAS Ctlgrs397507751
Max Magnitude0
ClinVar
Risk rs397507751(;)
Alt rs397507751(;)
Reference rs397507751(AC;AC)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913432_32913433delCA
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000044528.2, RCV000077342.2, RCV000132504.2,