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rs397507657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507657(-;-)
Make rs397507657(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337550
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507657
ebirs397507657
HLIrs397507657
Exacrs397507657
Varsomers397507657
Maprs397507657
PheGenIrs397507657
hapmaprs397507657
1000 genomesrs397507657
hgdprs397507657
ensemblrs397507657
gopubmedrs397507657
geneviewrs397507657
scholarrs397507657
googlers397507657
pharmgkbrs397507657
gwascentralrs397507657
openSNPrs397507657
23andMers397507657
23andMe allrs397507657
SNP Nexus

SNPshotrs397507657
SNPdbers397507657
MSV3drs397507657
GWAS Ctlgrs397507657
Max Magnitude0
ClinVar
Risk rs397507657(;)
Alt rs397507657(;)
Reference rs397507657(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32911687delT
CLNSRC ClinVar
CLNACC RCV000044144.2, RCV000166884.1,