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rs397507910

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507910(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355156
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507910
dbSNP (old)rs397507910
ClinGenrs397507910
ebirs397507910
HLIrs397507910
Exacrs397507910
Varsomers397507910
Maprs397507910
PheGenIrs397507910
Biobankrs397507910
1000 genomesrs397507910
hgdprs397507910
ensemblrs397507910
gopubmedrs397507910
geneviewrs397507910
scholarrs397507910
googlers397507910
pharmgkbrs397507910
gwascentralrs397507910
openSNPrs397507910
23andMers397507910
23andMe allrs397507910
SNP Nexus

SNPshotrs397507910
SNPdbers397507910
MSV3drs397507910
GWAS Ctlgrs397507910
Max Magnitude6
ClinVar
Risk rs397507910(G;G) rs397507910(T;T)
Alt rs397507910(G;G) rs397507910(T;T)
Reference Rs397507910(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.32929293C>T
CLNSRC ClinVar
CLNACC RCV000045183.2, RCV000257341.2,