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rs397507647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs397507647(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337267
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507647
dbSNP (old)rs397507647
ClinGenrs397507647
ebirs397507647
HLIrs397507647
Exacrs397507647
Gnomadrs397507647
Varsomers397507647
Maprs397507647
PheGenIrs397507647
Biobankrs397507647
1000 genomesrs397507647
hgdprs397507647
ensemblrs397507647
gopubmedrs397507647
geneviewrs397507647
scholarrs397507647
googlers397507647
pharmgkbrs397507647
gwascentralrs397507647
openSNPrs397507647
23andMers397507647
23andMe allrs397507647
SNP Nexus

SNPshotrs397507647
SNPdbers397507647
MSV3drs397507647
GWAS Ctlgrs397507647
Max Magnitude6
ClinVar
Risk rs397507647(G;G)
Alt rs397507647(G;G)
Reference Rs397507647(T;T)
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.32911404T>G
CLNSRC ClinVar
CLNACC RCV000044084.2, RCV000257832.2,