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rs397507631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507631(G;G)
Make rs397507631(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336826
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507631
ebirs397507631
HLIrs397507631
Exacrs397507631
Varsomers397507631
Maprs397507631
PheGenIrs397507631
hapmaprs397507631
1000 genomesrs397507631
hgdprs397507631
ensemblrs397507631
gopubmedrs397507631
geneviewrs397507631
scholarrs397507631
googlers397507631
pharmgkbrs397507631
gwascentralrs397507631
openSNPrs397507631
23andMers397507631
23andMe allrs397507631
SNP Nexus

SNPshotrs397507631
SNPdbers397507631
MSV3drs397507631
GWAS Ctlgrs397507631
Max Magnitude0
ClinVar
Risk rs397507631(C,G;C,G)
Alt rs397507631(C,G;C,G)
Reference rs397507631(T;T)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32910963T>C; NC_000013.10:g.32910963T>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000120343.1, RCV000130598.2, RCV000044003.3,