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rs397507737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507737(C;T)
Make rs397507737(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339039
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507737
ebirs397507737
HLIrs397507737
Exacrs397507737
Varsomers397507737
Maprs397507737
PheGenIrs397507737
hapmaprs397507737
1000 genomesrs397507737
hgdprs397507737
ensemblrs397507737
gopubmedrs397507737
geneviewrs397507737
scholarrs397507737
googlers397507737
pharmgkbrs397507737
gwascentralrs397507737
openSNPrs397507737
23andMers397507737
23andMe allrs397507737
SNP Nexus

SNPshotrs397507737
SNPdbers397507737
MSV3drs397507737
GWAS Ctlgrs397507737
Max Magnitude0
ClinVar
Risk rs397507737(T;T)
Alt rs397507737(T;T)
Reference rs397507737(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913176C>T
CLNSRC ClinVar
CLNACC RCV000044470.2,