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rs587781436

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781436(-;-)
Make rs587781436(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337706
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781436
ebirs587781436
HLIrs587781436
Exacrs587781436
Varsomers587781436
Maprs587781436
PheGenIrs587781436
hapmaprs587781436
1000 genomesrs587781436
hgdprs587781436
ensemblrs587781436
gopubmedrs587781436
geneviewrs587781436
scholarrs587781436
googlers587781436
pharmgkbrs587781436
gwascentralrs587781436
openSNPrs587781436
23andMers587781436
23andMe allrs587781436
SNP Nexus

SNPshotrs587781436
SNPdbers587781436
MSV3drs587781436
GWAS Ctlgrs587781436
Max Magnitude0
ClinVar
Risk rs587781436(;)
Alt rs587781436(;)
Reference rs587781436(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32911843delA
CLNSRC
CLNACC RCV000129333.2,