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rs587782011

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782011(-;-)
Make rs587782011(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339912
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782011
ebirs587782011
HLIrs587782011
Exacrs587782011
Varsomers587782011
Maprs587782011
PheGenIrs587782011
hapmaprs587782011
1000 genomesrs587782011
hgdprs587782011
ensemblrs587782011
gopubmedrs587782011
geneviewrs587782011
scholarrs587782011
googlers587782011
pharmgkbrs587782011
gwascentralrs587782011
openSNPrs587782011
23andMers587782011
23andMe allrs587782011
SNP Nexus

SNPshotrs587782011
SNPdbers587782011
MSV3drs587782011
GWAS Ctlgrs587782011
Max Magnitude0
ClinVar
Risk rs587782011(;)
Alt rs587782011(;)
Reference rs587782011(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914049delT
CLNSRC
CLNACC RCV000130434.2,