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rs397507351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507351(-;-)
Make rs397507351(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339791
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507351
ebirs397507351
HLIrs397507351
Exacrs397507351
Varsomers397507351
Maprs397507351
PheGenIrs397507351
hapmaprs397507351
1000 genomesrs397507351
hgdprs397507351
ensemblrs397507351
gopubmedrs397507351
geneviewrs397507351
scholarrs397507351
googlers397507351
pharmgkbrs397507351
gwascentralrs397507351
openSNPrs397507351
23andMers397507351
23andMe allrs397507351
SNP Nexus

SNPshotrs397507351
SNPdbers397507351
MSV3drs397507351
GWAS Ctlgrs397507351
Max Magnitude0
ClinVar
Risk rs397507351(;)
Alt rs397507351(;)
Reference rs397507351(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913928delA
CLNSRC ClinVar
CLNACC RCV000031546.3,