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rs587781585

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587781585(-;-)
Make rs587781585(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339777
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781585
ebirs587781585
HLIrs587781585
Exacrs587781585
Varsomers587781585
Maprs587781585
PheGenIrs587781585
hapmaprs587781585
1000 genomesrs587781585
hgdprs587781585
ensemblrs587781585
gopubmedrs587781585
geneviewrs587781585
scholarrs587781585
googlers587781585
pharmgkbrs587781585
gwascentralrs587781585
openSNPrs587781585
23andMers587781585
23andMe allrs587781585
SNP Nexus

SNPshotrs587781585
SNPdbers587781585
MSV3drs587781585
GWAS Ctlgrs587781585
Max Magnitude0
ClinVar
Risk rs587781585(;)
Alt rs587781585(;)
Reference rs587781585(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913914_32913915delAT
CLNSRC
CLNACC RCV000129625.2,