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rs397507889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507889(-;-)
Make rs397507889(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346885
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507889
ebirs397507889
HLIrs397507889
Exacrs397507889
Varsomers397507889
Maprs397507889
PheGenIrs397507889
hapmaprs397507889
1000 genomesrs397507889
hgdprs397507889
ensemblrs397507889
gopubmedrs397507889
geneviewrs397507889
scholarrs397507889
googlers397507889
pharmgkbrs397507889
gwascentralrs397507889
openSNPrs397507889
23andMers397507889
23andMe allrs397507889
SNP Nexus

SNPshotrs397507889
SNPdbers397507889
MSV3drs397507889
GWAS Ctlgrs397507889
Max Magnitude0
ClinVar
Risk rs397507889(;)
Alt rs397507889(;)
Reference rs397507889(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.32921022delT
CLNSRC ClinVar
CLNACC RCV000045105.2,