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rs587782378

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587782378(-;-)
Make rs587782378(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32380083
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782378
ebirs587782378
HLIrs587782378
Exacrs587782378
Varsomers587782378
Maprs587782378
PheGenIrs587782378
hapmaprs587782378
1000 genomesrs587782378
hgdprs587782378
ensemblrs587782378
gopubmedrs587782378
geneviewrs587782378
scholarrs587782378
googlers587782378
pharmgkbrs587782378
gwascentralrs587782378
openSNPrs587782378
23andMers587782378
23andMe allrs587782378
SNP Nexus

SNPshotrs587782378
SNPdbers587782378
MSV3drs587782378
GWAS Ctlgrs587782378
Max Magnitude0
ClinVar
Risk rs587782378(;)
Alt rs587782378(;)
Reference rs587782378(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32954220_32954221delTT
CLNSRC
CLNACC RCV000131371.2,