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rs397507304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507304(-;-)
Make rs397507304(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337537
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507304
ebirs397507304
HLIrs397507304
Exacrs397507304
Varsomers397507304
Maprs397507304
PheGenIrs397507304
hapmaprs397507304
1000 genomesrs397507304
hgdprs397507304
ensemblrs397507304
gopubmedrs397507304
geneviewrs397507304
scholarrs397507304
googlers397507304
pharmgkbrs397507304
gwascentralrs397507304
openSNPrs397507304
23andMers397507304
23andMe allrs397507304
SNP Nexus

SNPshotrs397507304
SNPdbers397507304
MSV3drs397507304
GWAS Ctlgrs397507304
Max Magnitude0
ClinVar
Risk rs397507304(;)
Alt rs397507304(;)
Reference rs397507304(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.32911674delA
CLNSRC ClinVar
CLNACC RCV000031408.3,