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rs397507972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507972(-;-)
Make rs397507972(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363487
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507972
ebirs397507972
HLIrs397507972
Exacrs397507972
Varsomers397507972
Maprs397507972
PheGenIrs397507972
hapmaprs397507972
1000 genomesrs397507972
hgdprs397507972
ensemblrs397507972
gopubmedrs397507972
geneviewrs397507972
scholarrs397507972
googlers397507972
pharmgkbrs397507972
gwascentralrs397507972
openSNPrs397507972
23andMers397507972
23andMe allrs397507972
SNP Nexus

SNPshotrs397507972
SNPdbers397507972
MSV3drs397507972
GWAS Ctlgrs397507972
Max Magnitude0
ClinVar
Risk rs397507972(;)
Alt rs397507972(;)
Reference rs397507972(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.32937624delC
CLNSRC ClinVar
CLNACC RCV000045465.2,