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rs397507629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507629(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336810
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507629
dbSNP (old)rs397507629
ClinGenrs397507629
ebirs397507629
HLIrs397507629
Exacrs397507629
Gnomadrs397507629
Varsomers397507629
Maprs397507629
PheGenIrs397507629
Biobankrs397507629
1000 genomesrs397507629
hgdprs397507629
ensemblrs397507629
gopubmedrs397507629
geneviewrs397507629
scholarrs397507629
googlers397507629
pharmgkbrs397507629
gwascentralrs397507629
openSNPrs397507629
23andMers397507629
23andMe allrs397507629
SNP Nexus

SNPshotrs397507629
SNPdbers397507629
MSV3drs397507629
GWAS Ctlgrs397507629
Max Magnitude6
ClinVar
Risk rs397507629(T;T)
Alt rs397507629(T;T)
Reference Rs397507629(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910947C>T
CLNSRC ClinVar
CLNACC RCV000043999.2, RCV000257203.2,