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rs397507384

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507384(C;T)
Make rs397507384(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355088
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507384
ebirs397507384
HLIrs397507384
Exacrs397507384
Varsomers397507384
Maprs397507384
PheGenIrs397507384
hapmaprs397507384
1000 genomesrs397507384
hgdprs397507384
ensemblrs397507384
gopubmedrs397507384
geneviewrs397507384
scholarrs397507384
googlers397507384
pharmgkbrs397507384
gwascentralrs397507384
openSNPrs397507384
23andMers397507384
23andMe allrs397507384
SNP Nexus

SNPshotrs397507384
SNPdbers397507384
MSV3drs397507384
GWAS Ctlgrs397507384
Max Magnitude0
ClinVar
Risk rs397507384(T;T)
Alt rs397507384(T;T)
Reference rs397507384(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929225C>T
CLNSRC ClinVar
CLNACC RCV000031670.3,