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rs397507639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507639(-;-)
Make rs397507639(-;T)
Make rs397507639(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337120
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507639
ebirs397507639
HLIrs397507639
Exacrs397507639
Varsomers397507639
Maprs397507639
PheGenIrs397507639
hapmaprs397507639
1000 genomesrs397507639
hgdprs397507639
ensemblrs397507639
gopubmedrs397507639
geneviewrs397507639
scholarrs397507639
googlers397507639
pharmgkbrs397507639
gwascentralrs397507639
openSNPrs397507639
23andMers397507639
23andMe allrs397507639
SNP Nexus

SNPshotrs397507639
SNPdbers397507639
MSV3drs397507639
GWAS Ctlgrs397507639
Max Magnitude0
ClinVar
Risk rs397507639(T;T)
Alt rs397507639(T;T)
Reference rs397507639(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911257dupT
CLNSRC ClinVar
CLNACC RCV000044050.2,