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rs587781639

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781639(-;-)
Make rs587781639(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61801311
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781639
ebirs587781639
HLIrs587781639
Exacrs587781639
Varsomers587781639
Maprs587781639
PheGenIrs587781639
hapmaprs587781639
1000 genomesrs587781639
hgdprs587781639
ensemblrs587781639
gopubmedrs587781639
geneviewrs587781639
scholarrs587781639
googlers587781639
pharmgkbrs587781639
gwascentralrs587781639
openSNPrs587781639
23andMers587781639
23andMe allrs587781639
SNP Nexus

SNPshotrs587781639
SNPdbers587781639
MSV3drs587781639
GWAS Ctlgrs587781639
Max Magnitude0
ClinVar
Risk rs587781639(;)
Alt rs587781639(;)
Reference rs587781639(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59878672delT
CLNSRC
CLNACC RCV000129762.2,