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rs587782075

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782075(-;-)
Make rs587782075(-;TA)
Make rs587782075(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339527
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782075
ebirs587782075
HLIrs587782075
Exacrs587782075
Varsomers587782075
Maprs587782075
PheGenIrs587782075
hapmaprs587782075
1000 genomesrs587782075
hgdprs587782075
ensemblrs587782075
gopubmedrs587782075
geneviewrs587782075
scholarrs587782075
googlers587782075
pharmgkbrs587782075
gwascentralrs587782075
openSNPrs587782075
23andMers587782075
23andMe allrs587782075
SNP Nexus

SNPshotrs587782075
SNPdbers587782075
MSV3drs587782075
GWAS Ctlgrs587782075
Max Magnitude0
ClinVar
Risk rs587782075(TA;TA)
Alt rs587782075(TA;TA)
Reference rs587782075(;)
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.32913663_32913664dupTA
CLNSRC
CLNACC RCV000130567.2, RCV000211017.1,