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rs587781945

From SNPedia

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


Make rs587781945(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32326104
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781945
dbSNP (old)rs587781945
ClinGenrs587781945
ebirs587781945
HLIrs587781945
Exacrs587781945
Varsomers587781945
Maprs587781945
PheGenIrs587781945
Biobankrs587781945
1000 genomesrs587781945
hgdprs587781945
ensemblrs587781945
gopubmedrs587781945
geneviewrs587781945
scholarrs587781945
googlers587781945
pharmgkbrs587781945
gwascentralrs587781945
openSNPrs587781945
23andMers587781945
23andMe allrs587781945
SNP Nexus

SNPshotrs587781945
SNPdbers587781945
MSV3drs587781945
GWAS Ctlgrs587781945
Max Magnitude6
ClinVar
Risk rs587781945(-;-)
Alt rs587781945(-;-)
Reference Rs587781945(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32900241delT
CLNSRC
CLNACC RCV000130313.2, RCV000241112.1,