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rs397508049

From SNPedia

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


Make rs397508049(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394825
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508049
dbSNP (old)rs397508049
ClinGenrs397508049
ebirs397508049
HLIrs397508049
Exacrs397508049
Gnomadrs397508049
Varsomers397508049
Maprs397508049
PheGenIrs397508049
Biobankrs397508049
1000 genomesrs397508049
hgdprs397508049
ensemblrs397508049
gopubmedrs397508049
geneviewrs397508049
scholarrs397508049
googlers397508049
pharmgkbrs397508049
gwascentralrs397508049
openSNPrs397508049
23andMers397508049
23andMe allrs397508049
SNP Nexus

SNPshotrs397508049
SNPdbers397508049
MSV3drs397508049
GWAS Ctlgrs397508049
Max Magnitude6
ClinVar
Risk rs397508049(-;-)
Alt rs397508049(-;-)
Reference Rs397508049(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.32968962delC
CLNSRC ClinVar
CLNACC RCV000045809.2, RCV000257380.2,