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rs397507571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507571(G;T)
Make rs397507571(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316470
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507571
ebirs397507571
HLIrs397507571
Exacrs397507571
Varsomers397507571
Maprs397507571
PheGenIrs397507571
hapmaprs397507571
1000 genomesrs397507571
hgdprs397507571
ensemblrs397507571
gopubmedrs397507571
geneviewrs397507571
scholarrs397507571
googlers397507571
pharmgkbrs397507571
gwascentralrs397507571
openSNPrs397507571
23andMers397507571
23andMe allrs397507571
SNP Nexus

SNPshotrs397507571
SNPdbers397507571
MSV3drs397507571
GWAS Ctlgrs397507571
Max Magnitude0
ClinVar
Risk rs397507571(T;T)
Alt rs397507571(T;T)
Reference rs397507571(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast not specified
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast not specified
Reversed 0
HGVS NC_000013.10:g.32890607G>T
CLNSRC ClinVar
CLNACC RCV000043737.2, RCV000239090.1,