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rs587780651

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780651(-;-)
Make rs587780651(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32338132
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587780651
ebirs587780651
HLIrs587780651
Exacrs587780651
Varsomers587780651
Maprs587780651
PheGenIrs587780651
hapmaprs587780651
1000 genomesrs587780651
hgdprs587780651
ensemblrs587780651
gopubmedrs587780651
geneviewrs587780651
scholarrs587780651
googlers587780651
pharmgkbrs587780651
gwascentralrs587780651
openSNPrs587780651
23andMers587780651
23andMe allrs587780651
SNP Nexus

SNPshotrs587780651
SNPdbers587780651
MSV3drs587780651
GWAS Ctlgrs587780651
Max Magnitude0
ClinVar
Risk rs587780651(;)
Alt rs587780651(;)
Reference rs587780651(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32912271delT
CLNSRC
CLNACC RCV000082919.2, RCV000122909.1,