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rs397507977

From SNPedia

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


Make rs397507977(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363529
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507977
ebirs397507977
HLIrs397507977
Exacrs397507977
Varsomers397507977
Maprs397507977
PheGenIrs397507977
hapmaprs397507977
1000 genomesrs397507977
hgdprs397507977
ensemblrs397507977
gopubmedrs397507977
geneviewrs397507977
scholarrs397507977
googlers397507977
pharmgkbrs397507977
gwascentralrs397507977
openSNPrs397507977
23andMers397507977
23andMe allrs397507977
SNP Nexus

SNPshotrs397507977
SNPdbers397507977
MSV3drs397507977
GWAS Ctlgrs397507977
Max Magnitude6
ClinVar
Risk rs397507977(G;G)
Alt rs397507977(G;G)
Reference rs397507977(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937666T>G
CLNSRC ClinVar
CLNACC RCV000045475.2,