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rs587781772

From SNPedia

Orientationplus
Geno Mag Summary
(AGAA;AGAA) 0 common in clinvar
Make rs587781772(-;-)
Make rs587781772(-;AAGA)
Make rs587781772(AAGA;AAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32398283
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781772
ebirs587781772
HLIrs587781772
Exacrs587781772
Varsomers587781772
Maprs587781772
PheGenIrs587781772
hapmaprs587781772
1000 genomesrs587781772
hgdprs587781772
ensemblrs587781772
gopubmedrs587781772
geneviewrs587781772
scholarrs587781772
googlers587781772
pharmgkbrs587781772
gwascentralrs587781772
openSNPrs587781772
23andMers587781772
23andMe allrs587781772
SNP Nexus

SNPshotrs587781772
SNPdbers587781772
MSV3drs587781772
GWAS Ctlgrs587781772
Max Magnitude0
ClinVar
Risk rs587781772(;)
Alt rs587781772(;)
Reference rs587781772(AGAA;AGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32972420_32972423delAAGA
CLNSRC
CLNACC RCV000130006.2,