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rs397508019

From SNPedia

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


Make rs397508019(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379477
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508019
ClinGenrs397508019
ebirs397508019
HLIrs397508019
Exacrs397508019
Varsomers397508019
Maprs397508019
PheGenIrs397508019
hapmaprs397508019
1000 genomesrs397508019
hgdprs397508019
ensemblrs397508019
gopubmedrs397508019
geneviewrs397508019
scholarrs397508019
googlers397508019
pharmgkbrs397508019
gwascentralrs397508019
openSNPrs397508019
23andMers397508019
23andMe allrs397508019
SNP Nexus

SNPshotrs397508019
SNPdbers397508019
MSV3drs397508019
GWAS Ctlgrs397508019
Max Magnitude6
ClinVar
Risk rs397508019(-;-)
Alt rs397508019(-;-)
Reference Rs397508019(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953614delT
CLNSRC ClinVar
CLNACC RCV000045655.3, RCV000257384.2,