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rs397507424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507424(-;-)
Make rs397507424(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394706
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507424
ebirs397507424
HLIrs397507424
Exacrs397507424
Varsomers397507424
Maprs397507424
PheGenIrs397507424
hapmaprs397507424
1000 genomesrs397507424
hgdprs397507424
ensemblrs397507424
gopubmedrs397507424
geneviewrs397507424
scholarrs397507424
googlers397507424
pharmgkbrs397507424
gwascentralrs397507424
openSNPrs397507424
23andMers397507424
23andMe allrs397507424
SNP Nexus

SNPshotrs397507424
SNPdbers397507424
MSV3drs397507424
GWAS Ctlgrs397507424
Max Magnitude0
ClinVar
Risk rs397507424(;)
Alt rs397507424(;)
Reference rs397507424(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32968843delT
CLNSRC ClinVar
CLNACC RCV000031809.3,