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rs397507765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507765(-;-)
Make rs397507765(-;AGTAC)
Make rs397507765(AGTAC;AGTAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339523
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507765
ebirs397507765
HLIrs397507765
Exacrs397507765
Varsomers397507765
Maprs397507765
PheGenIrs397507765
hapmaprs397507765
1000 genomesrs397507765
hgdprs397507765
ensemblrs397507765
gopubmedrs397507765
geneviewrs397507765
scholarrs397507765
googlers397507765
pharmgkbrs397507765
gwascentralrs397507765
openSNPrs397507765
23andMers397507765
23andMe allrs397507765
SNP Nexus

SNPshotrs397507765
SNPdbers397507765
MSV3drs397507765
GWAS Ctlgrs397507765
Max Magnitude0
ClinVar
Risk rs397507765(ACAGT;ACAGT)
Alt rs397507765(ACAGT;ACAGT)
Reference rs397507765(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913656_32913660dupAGTAC
CLNSRC ClinVar
CLNACC RCV000044580.2,