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rs397507969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507969(-;-)
Make rs397507969(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363409
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507969
ebirs397507969
HLIrs397507969
Exacrs397507969
Varsomers397507969
Maprs397507969
PheGenIrs397507969
hapmaprs397507969
1000 genomesrs397507969
hgdprs397507969
ensemblrs397507969
gopubmedrs397507969
geneviewrs397507969
scholarrs397507969
googlers397507969
pharmgkbrs397507969
gwascentralrs397507969
openSNPrs397507969
23andMers397507969
23andMe allrs397507969
SNP Nexus

SNPshotrs397507969
SNPdbers397507969
MSV3drs397507969
GWAS Ctlgrs397507969
Max Magnitude0
ClinVar
Risk rs397507969(;)
Alt rs397507969(;)
Reference rs397507969(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.32937546delT
CLNSRC ClinVar
CLNACC RCV000045452.2,