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rs397507576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507576(A;A)
Make rs397507576(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332719
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507576
ebirs397507576
HLIrs397507576
Exacrs397507576
Varsomers397507576
Maprs397507576
PheGenIrs397507576
hapmaprs397507576
1000 genomesrs397507576
hgdprs397507576
ensemblrs397507576
gopubmedrs397507576
geneviewrs397507576
scholarrs397507576
googlers397507576
pharmgkbrs397507576
gwascentralrs397507576
openSNPrs397507576
23andMers397507576
23andMe allrs397507576
SNP Nexus

SNPshotrs397507576
SNPdbers397507576
MSV3drs397507576
GWAS Ctlgrs397507576
Max Magnitude0
ClinVar
Risk rs397507576(A;A)
Alt rs397507576(A;A)
Reference rs397507576(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.32906856T>A
CLNSRC ClinVar
CLNACC RCV000043765.2,