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rs397507569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507569(-;-)
Make rs397507569(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332560
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507569
ebirs397507569
HLIrs397507569
Exacrs397507569
Varsomers397507569
Maprs397507569
PheGenIrs397507569
hapmaprs397507569
1000 genomesrs397507569
hgdprs397507569
ensemblrs397507569
gopubmedrs397507569
geneviewrs397507569
scholarrs397507569
googlers397507569
pharmgkbrs397507569
gwascentralrs397507569
openSNPrs397507569
23andMers397507569
23andMe allrs397507569
SNP Nexus

SNPshotrs397507569
SNPdbers397507569
MSV3drs397507569
GWAS Ctlgrs397507569
Max Magnitude0
ClinVar
Risk rs397507569(;)
Alt rs397507569(;)
Reference rs397507569(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906697delA
CLNSRC ClinVar
CLNACC RCV000043735.2,