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rs397507776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507776(-;-)
Make rs397507776(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339605
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507776
ClinGenrs397507776
ebirs397507776
HLIrs397507776
Exacrs397507776
Varsomers397507776
Maprs397507776
PheGenIrs397507776
hapmaprs397507776
1000 genomesrs397507776
hgdprs397507776
ensemblrs397507776
gopubmedrs397507776
geneviewrs397507776
scholarrs397507776
googlers397507776
pharmgkbrs397507776
gwascentralrs397507776
openSNPrs397507776
23andMers397507776
23andMe allrs397507776
SNP Nexus

SNPshotrs397507776
SNPdbers397507776
MSV3drs397507776
GWAS Ctlgrs397507776
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507776(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913742delC
CLNSRC ClinVar
CLNACC RCV000044620.2,