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rs587782672

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782672(-;-)
Make rs587782672(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337713
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782672
ebirs587782672
HLIrs587782672
Exacrs587782672
Varsomers587782672
Maprs587782672
PheGenIrs587782672
hapmaprs587782672
1000 genomesrs587782672
hgdprs587782672
ensemblrs587782672
gopubmedrs587782672
geneviewrs587782672
scholarrs587782672
googlers587782672
pharmgkbrs587782672
gwascentralrs587782672
openSNPrs587782672
23andMers587782672
23andMe allrs587782672
SNP Nexus

SNPshotrs587782672
SNPdbers587782672
MSV3drs587782672
GWAS Ctlgrs587782672
Max Magnitude0
ClinVar
Risk rs587782672(;)
Alt rs587782672(;)
Reference rs587782672(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32911850delG
CLNSRC
CLNACC RCV000132095.2,