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rs397507764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507764(A;A)
Make rs397507764(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326284
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507764
ebirs397507764
HLIrs397507764
Exacrs397507764
Varsomers397507764
Maprs397507764
PheGenIrs397507764
hapmaprs397507764
1000 genomesrs397507764
hgdprs397507764
ensemblrs397507764
gopubmedrs397507764
geneviewrs397507764
scholarrs397507764
googlers397507764
pharmgkbrs397507764
gwascentralrs397507764
openSNPrs397507764
23andMers397507764
23andMe allrs397507764
SNP Nexus

SNPshotrs397507764
SNPdbers397507764
MSV3drs397507764
GWAS Ctlgrs397507764
Max Magnitude0
ClinVar
Risk rs397507764(A;A)
Alt rs397507764(A;A)
Reference rs397507764(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.32900421T>A
CLNSRC ClinVar
CLNACC RCV000044577.2,