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rs397507953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507953(-;-)
Make rs397507953(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363223
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507953
ebirs397507953
HLIrs397507953
Exacrs397507953
Varsomers397507953
Maprs397507953
PheGenIrs397507953
hapmaprs397507953
1000 genomesrs397507953
hgdprs397507953
ensemblrs397507953
gopubmedrs397507953
geneviewrs397507953
scholarrs397507953
googlers397507953
pharmgkbrs397507953
gwascentralrs397507953
openSNPrs397507953
23andMers397507953
23andMe allrs397507953
SNP Nexus

SNPshotrs397507953
SNPdbers397507953
MSV3drs397507953
GWAS Ctlgrs397507953
Max Magnitude0
ClinVar
Risk rs397507953(;)
Alt rs397507953(;)
Reference rs397507953(A;A)
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.32937360delA
CLNSRC ClinVar
CLNACC RCV000045389.2, RCV000238781.1,