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rs397507975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507975(G;T)
Make rs397507975(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363516
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507975
ebirs397507975
HLIrs397507975
Exacrs397507975
Varsomers397507975
Maprs397507975
PheGenIrs397507975
hapmaprs397507975
1000 genomesrs397507975
hgdprs397507975
ensemblrs397507975
gopubmedrs397507975
geneviewrs397507975
scholarrs397507975
googlers397507975
pharmgkbrs397507975
gwascentralrs397507975
openSNPrs397507975
23andMers397507975
23andMe allrs397507975
SNP Nexus

SNPshotrs397507975
SNPdbers397507975
MSV3drs397507975
GWAS Ctlgrs397507975
Max Magnitude0
ClinVar
Risk rs397507975(A,T;A,T)
Alt rs397507975(A,T;A,T)
Reference rs397507975(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937653G>A; NC_000013.10:g.32937653G>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000130828.2, RCV000045469.2, RCV000166747.1,