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rs397507954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507954(A;G)
Make rs397507954(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363225
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507954
ebirs397507954
HLIrs397507954
Exacrs397507954
Varsomers397507954
Maprs397507954
PheGenIrs397507954
hapmaprs397507954
1000 genomesrs397507954
hgdprs397507954
ensemblrs397507954
gopubmedrs397507954
geneviewrs397507954
scholarrs397507954
googlers397507954
pharmgkbrs397507954
gwascentralrs397507954
openSNPrs397507954
23andMers397507954
23andMe allrs397507954
SNP Nexus

SNPshotrs397507954
SNPdbers397507954
MSV3drs397507954
GWAS Ctlgrs397507954
Max Magnitude0
ClinVar
Risk rs397507954(G;G)
Alt rs397507954(G;G)
Reference rs397507954(A;A)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32937362A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045390.3, RCV000132001.2,