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rs587779358

From SNPedia

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Geno Mag Summary
(CGA;CGA) 0 common in clinvar
Make rs587779358(CGA;TTT)
Make rs587779358(TTT;TTT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333295
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587779358
ebirs587779358
HLIrs587779358
Exacrs587779358
Varsomers587779358
Maprs587779358
PheGenIrs587779358
hapmaprs587779358
1000 genomesrs587779358
hgdprs587779358
ensemblrs587779358
gopubmedrs587779358
geneviewrs587779358
scholarrs587779358
googlers587779358
pharmgkbrs587779358
gwascentralrs587779358
openSNPrs587779358
23andMers587779358
23andMe allrs587779358
SNP Nexus

SNPshotrs587779358
SNPdbers587779358
MSV3drs587779358
GWAS Ctlgrs587779358
Max Magnitude0
ClinVar
Risk rs587779358(TTT;TTT)
Alt rs587779358(TTT;TTT)
Reference rs587779358(CGA;CGA)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907432_32907434delCGAinsTTT
CLNSRC
CLNACC RCV000074518.1,