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rs397507638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507638(A;A)
Make rs397507638(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337103
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507638
ebirs397507638
HLIrs397507638
Exacrs397507638
Varsomers397507638
Maprs397507638
PheGenIrs397507638
hapmaprs397507638
1000 genomesrs397507638
hgdprs397507638
ensemblrs397507638
gopubmedrs397507638
geneviewrs397507638
scholarrs397507638
googlers397507638
pharmgkbrs397507638
gwascentralrs397507638
openSNPrs397507638
23andMers397507638
23andMe allrs397507638
SNP Nexus

SNPshotrs397507638
SNPdbers397507638
MSV3drs397507638
GWAS Ctlgrs397507638
Max Magnitude0
ClinVar
Risk rs397507638(A;A)
Alt rs397507638(A;A)
Reference rs397507638(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911240T>A
CLNSRC ClinVar
CLNACC RCV000044047.2,