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rs397507877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507877(-;-)
Make rs397507877(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341043
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507877
ebirs397507877
HLIrs397507877
Exacrs397507877
Varsomers397507877
Maprs397507877
PheGenIrs397507877
hapmaprs397507877
1000 genomesrs397507877
hgdprs397507877
ensemblrs397507877
gopubmedrs397507877
geneviewrs397507877
scholarrs397507877
googlers397507877
pharmgkbrs397507877
gwascentralrs397507877
openSNPrs397507877
23andMers397507877
23andMe allrs397507877
SNP Nexus

SNPshotrs397507877
SNPdbers397507877
MSV3drs397507877
GWAS Ctlgrs397507877
Max Magnitude0
ClinVar
Risk rs397507877(;)
Alt rs397507877(;)
Reference rs397507877(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.32915180delA
CLNSRC ClinVar
CLNACC RCV000045019.2,