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rs587779363

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779363(-;-)
Make rs587779363(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339550
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587779363
ebirs587779363
HLIrs587779363
Exacrs587779363
Varsomers587779363
Maprs587779363
PheGenIrs587779363
hapmaprs587779363
1000 genomesrs587779363
hgdprs587779363
ensemblrs587779363
gopubmedrs587779363
geneviewrs587779363
scholarrs587779363
googlers587779363
pharmgkbrs587779363
gwascentralrs587779363
openSNPrs587779363
23andMers587779363
23andMe allrs587779363
SNP Nexus

SNPshotrs587779363
SNPdbers587779363
MSV3drs587779363
GWAS Ctlgrs587779363
Max Magnitude0
ClinVar
Risk rs587779363(;)
Alt rs587779363(;)
Reference rs587779363(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913687delT
CLNSRC
CLNACC RCV000074535.3, RCV000077349.2,