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rs397507619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507619(A;TT)
Make rs397507619(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319224
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507619
ebirs397507619
HLIrs397507619
Exacrs397507619
Varsomers397507619
Maprs397507619
PheGenIrs397507619
hapmaprs397507619
1000 genomesrs397507619
hgdprs397507619
ensemblrs397507619
gopubmedrs397507619
geneviewrs397507619
scholarrs397507619
googlers397507619
pharmgkbrs397507619
gwascentralrs397507619
openSNPrs397507619
23andMers397507619
23andMe allrs397507619
SNP Nexus

SNPshotrs397507619
SNPdbers397507619
MSV3drs397507619
GWAS Ctlgrs397507619
Max Magnitude0
ClinVar
Risk rs397507619(TT;TT)
Alt rs397507619(TT;TT)
Reference rs397507619(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.32893361delAinsTT
CLNSRC ClinVar
CLNACC RCV000043953.2, RCV000225535.1,