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rs397507673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGC;CAGC) 0 common in clinvar
Make rs397507673(-;-)
Make rs397507673(-;CAGC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337886
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507673
ebirs397507673
HLIrs397507673
Exacrs397507673
Varsomers397507673
Maprs397507673
PheGenIrs397507673
hapmaprs397507673
1000 genomesrs397507673
hgdprs397507673
ensemblrs397507673
gopubmedrs397507673
geneviewrs397507673
scholarrs397507673
googlers397507673
pharmgkbrs397507673
gwascentralrs397507673
openSNPrs397507673
23andMers397507673
23andMe allrs397507673
SNP Nexus

SNPshotrs397507673
SNPdbers397507673
MSV3drs397507673
GWAS Ctlgrs397507673
Max Magnitude0
ClinVar
Risk rs397507673(;)
Alt rs397507673(;)
Reference rs397507673(CAGC;CAGC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912023_32912026delCAGC
CLNSRC ClinVar
CLNACC RCV000044215.2,