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rs587781850

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781850(-;-)
Make rs587781850(-;G)
Make rs587781850(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337766
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781850
ebirs587781850
HLIrs587781850
Exacrs587781850
Varsomers587781850
Maprs587781850
PheGenIrs587781850
hapmaprs587781850
1000 genomesrs587781850
hgdprs587781850
ensemblrs587781850
gopubmedrs587781850
geneviewrs587781850
scholarrs587781850
googlers587781850
pharmgkbrs587781850
gwascentralrs587781850
openSNPrs587781850
23andMers587781850
23andMe allrs587781850
SNP Nexus

SNPshotrs587781850
SNPdbers587781850
MSV3drs587781850
GWAS Ctlgrs587781850
Max Magnitude0
ClinVar
Risk rs587781850(G;G)
Alt rs587781850(G;G)
Reference rs587781850(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32911903dupG
CLNSRC
CLNACC RCV000130156.2,