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rs397507320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507320(A;A)
Make rs397507320(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325155
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507320
ebirs397507320
HLIrs397507320
Exacrs397507320
Varsomers397507320
Maprs397507320
PheGenIrs397507320
hapmaprs397507320
1000 genomesrs397507320
hgdprs397507320
ensemblrs397507320
gopubmedrs397507320
geneviewrs397507320
scholarrs397507320
googlers397507320
pharmgkbrs397507320
gwascentralrs397507320
openSNPrs397507320
23andMers397507320
23andMe allrs397507320
SNP Nexus

SNPshotrs397507320
SNPdbers397507320
MSV3drs397507320
GWAS Ctlgrs397507320
Max Magnitude0
ClinVar
Risk rs397507320(A;A)
Alt rs397507320(A;A)
Reference rs397507320(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32899292T>A
CLNSRC ClinVar
CLNACC RCV000031450.4, RCV000044326.2,