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rs397507841

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507841(A;G)
Make rs397507841(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326617
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507841
ebirs397507841
HLIrs397507841
Exacrs397507841
Varsomers397507841
Maprs397507841
PheGenIrs397507841
hapmaprs397507841
1000 genomesrs397507841
hgdprs397507841
ensemblrs397507841
gopubmedrs397507841
geneviewrs397507841
scholarrs397507841
googlers397507841
pharmgkbrs397507841
gwascentralrs397507841
openSNPrs397507841
23andMers397507841
23andMe allrs397507841
SNP Nexus

SNPshotrs397507841
SNPdbers397507841
MSV3drs397507841
GWAS Ctlgrs397507841
Max Magnitude0
ClinVar
Risk rs397507841(G;G)
Alt rs397507841(G;G)
Reference rs397507841(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.32900754A>G
CLNSRC ClinVar
CLNACC RCV000044900.2,