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rs397507290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397507290(-;-)
Make rs397507290(-;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336973
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507290
ebirs397507290
HLIrs397507290
Exacrs397507290
Varsomers397507290
Maprs397507290
PheGenIrs397507290
hapmaprs397507290
1000 genomesrs397507290
hgdprs397507290
ensemblrs397507290
gopubmedrs397507290
geneviewrs397507290
scholarrs397507290
googlers397507290
pharmgkbrs397507290
gwascentralrs397507290
openSNPrs397507290
23andMers397507290
23andMe allrs397507290
SNP Nexus

SNPshotrs397507290
SNPdbers397507290
MSV3drs397507290
GWAS Ctlgrs397507290
Max Magnitude0
ClinVar
Risk rs397507290(;)
Alt rs397507290(;)
Reference rs397507290(AT;AT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911110_32911111delTA
CLNSRC ClinVar
CLNACC RCV000031376.3,