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rs397507396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs397507396(-;-)
Make rs397507396(-;CC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363407
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507396
ebirs397507396
HLIrs397507396
Exacrs397507396
Varsomers397507396
Maprs397507396
PheGenIrs397507396
hapmaprs397507396
1000 genomesrs397507396
hgdprs397507396
ensemblrs397507396
gopubmedrs397507396
geneviewrs397507396
scholarrs397507396
googlers397507396
pharmgkbrs397507396
gwascentralrs397507396
openSNPrs397507396
23andMers397507396
23andMe allrs397507396
SNP Nexus

SNPshotrs397507396
SNPdbers397507396
MSV3drs397507396
GWAS Ctlgrs397507396
Max Magnitude0
ClinVar
Risk rs397507396(;)
Alt rs397507396(;)
Reference rs397507396(CC;CC)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937544_32937545delCC
CLNSRC ClinVar
CLNACC RCV000031726.3,