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rs397507944

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507944(-;-)
Make rs397507944(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362643
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507944
ebirs397507944
HLIrs397507944
Exacrs397507944
Varsomers397507944
Maprs397507944
PheGenIrs397507944
hapmaprs397507944
1000 genomesrs397507944
hgdprs397507944
ensemblrs397507944
gopubmedrs397507944
geneviewrs397507944
scholarrs397507944
googlers397507944
pharmgkbrs397507944
gwascentralrs397507944
openSNPrs397507944
23andMers397507944
23andMe allrs397507944
SNP Nexus

SNPshotrs397507944
SNPdbers397507944
MSV3drs397507944
GWAS Ctlgrs397507944
Max Magnitude0
ClinVar
Risk rs397507944(;)
Alt rs397507944(;)
Reference rs397507944(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.32936780delT
CLNSRC ClinVar
CLNACC RCV000045343.2,