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rs587782514

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782514(G;G)
Make rs587782514(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61808581
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587782514
ebirs587782514
HLIrs587782514
Exacrs587782514
Varsomers587782514
Maprs587782514
PheGenIrs587782514
hapmaprs587782514
1000 genomesrs587782514
hgdprs587782514
ensemblrs587782514
gopubmedrs587782514
geneviewrs587782514
scholarrs587782514
googlers587782514
pharmgkbrs587782514
gwascentralrs587782514
openSNPrs587782514
23andMers587782514
23andMe allrs587782514
SNP Nexus

SNPshotrs587782514
SNPdbers587782514
MSV3drs587782514
GWAS Ctlgrs587782514
Max Magnitude0
ClinVar
Risk rs587782514(G;G)
Alt rs587782514(G;G)
Reference rs587782514(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59885942A>C
CLNSRC
CLNACC RCV000131664.2,