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rs397507665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507665(-;-)
Make rs397507665(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337721
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507665
ebirs397507665
HLIrs397507665
Exacrs397507665
Varsomers397507665
Maprs397507665
PheGenIrs397507665
hapmaprs397507665
1000 genomesrs397507665
hgdprs397507665
ensemblrs397507665
gopubmedrs397507665
geneviewrs397507665
scholarrs397507665
googlers397507665
pharmgkbrs397507665
gwascentralrs397507665
openSNPrs397507665
23andMers397507665
23andMe allrs397507665
SNP Nexus

SNPshotrs397507665
SNPdbers397507665
MSV3drs397507665
GWAS Ctlgrs397507665
Max Magnitude0
ClinVar
Risk rs397507665(;)
Alt rs397507665(;)
Reference rs397507665(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911858_32911859delAA
CLNSRC ClinVar
CLNACC RCV000044182.2,