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rs587782854

From SNPedia

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Geno Mag Summary
(TGA;TGA) 0 common in clinvar
Make rs587782854(C;C)
Make rs587782854(C;TGA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339176
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782854
ebirs587782854
HLIrs587782854
Exacrs587782854
Varsomers587782854
Maprs587782854
PheGenIrs587782854
hapmaprs587782854
1000 genomesrs587782854
hgdprs587782854
ensemblrs587782854
gopubmedrs587782854
geneviewrs587782854
scholarrs587782854
googlers587782854
pharmgkbrs587782854
gwascentralrs587782854
openSNPrs587782854
23andMers587782854
23andMe allrs587782854
SNP Nexus

SNPshotrs587782854
SNPdbers587782854
MSV3drs587782854
GWAS Ctlgrs587782854
Max Magnitude0
ClinVar
Risk rs587782854(C;C)
Alt rs587782854(C;C)
Reference rs587782854(TGA;TGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913313_32913315delTGAinsC
CLNSRC
CLNACC RCV000132458.2,