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rs397507867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507867(A;A)
Make rs397507867(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340912
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507867
ebirs397507867
HLIrs397507867
Exacrs397507867
Varsomers397507867
Maprs397507867
PheGenIrs397507867
hapmaprs397507867
1000 genomesrs397507867
hgdprs397507867
ensemblrs397507867
gopubmedrs397507867
geneviewrs397507867
scholarrs397507867
googlers397507867
pharmgkbrs397507867
gwascentralrs397507867
openSNPrs397507867
23andMers397507867
23andMe allrs397507867
SNP Nexus

SNPshotrs397507867
SNPdbers397507867
MSV3drs397507867
GWAS Ctlgrs397507867
Max Magnitude0
ClinVar
Risk rs397507867(A;A)
Alt rs397507867(A;A)
Reference rs397507867(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.32915049C>A
CLNSRC ClinVar
CLNACC RCV000044984.2,