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rs587782780

From SNPedia

Orientationplus
Geno Mag Summary
(GATTA;GATTA) 0 common in clinvar
Make rs587782780(-;-)
Make rs587782780(-;GATTA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336414
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782780
ebirs587782780
HLIrs587782780
Exacrs587782780
Varsomers587782780
Maprs587782780
PheGenIrs587782780
hapmaprs587782780
1000 genomesrs587782780
hgdprs587782780
ensemblrs587782780
gopubmedrs587782780
geneviewrs587782780
scholarrs587782780
googlers587782780
pharmgkbrs587782780
gwascentralrs587782780
openSNPrs587782780
23andMers587782780
23andMe allrs587782780
SNP Nexus

SNPshotrs587782780
SNPdbers587782780
MSV3drs587782780
GWAS Ctlgrs587782780
Max Magnitude0
ClinVar
Risk rs587782780(;)
Alt rs587782780(;)
Reference rs587782780(GATTA;GATTA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32910551_32910555delGATTA
CLNSRC
CLNACC RCV000132320.2,