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rs587782901

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782901(-;-)
Make rs587782901(-;T)
Make rs587782901(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340070
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782901
ebirs587782901
HLIrs587782901
Exacrs587782901
Varsomers587782901
Maprs587782901
PheGenIrs587782901
hapmaprs587782901
1000 genomesrs587782901
hgdprs587782901
ensemblrs587782901
gopubmedrs587782901
geneviewrs587782901
scholarrs587782901
googlers587782901
pharmgkbrs587782901
gwascentralrs587782901
openSNPrs587782901
23andMers587782901
23andMe allrs587782901
SNP Nexus

SNPshotrs587782901
SNPdbers587782901
MSV3drs587782901
GWAS Ctlgrs587782901
Max Magnitude0
ClinVar
Risk rs587782901(T;T)
Alt rs587782901(T;T)
Reference rs587782901(;)
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.32914207dupT
CLNSRC
CLNACC RCV000132544.2, RCV000239079.1,