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rs397508045

From SNPedia

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


Make rs397508045(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319101
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508045
dbSNP (old)rs397508045
ClinGenrs397508045
ebirs397508045
HLIrs397508045
Exacrs397508045
Gnomadrs397508045
Varsomers397508045
Maprs397508045
PheGenIrs397508045
Biobankrs397508045
1000 genomesrs397508045
hgdprs397508045
ensemblrs397508045
gopubmedrs397508045
geneviewrs397508045
scholarrs397508045
googlers397508045
pharmgkbrs397508045
gwascentralrs397508045
openSNPrs397508045
23andMers397508045
23andMe allrs397508045
SNP Nexus

SNPshotrs397508045
SNPdbers397508045
MSV3drs397508045
GWAS Ctlgrs397508045
Max Magnitude6
ClinVar
Risk rs397508045(A;A) rs397508045(T;T)
Alt rs397508045(A;A) rs397508045(T;T)
Reference Rs397508045(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Neoplasm of breast
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Neoplasm of breast
Reversed 0
HGVS NC_000013.10:g.32893238G>A; NC_000013.10:g.32893238G>T
CLNSRC ClinVar
CLNACC RCV000045785.3, RCV000241373.2, RCV000240757.1,