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rs587781985

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781985(-;-)
Make rs587781985(-;G)
Make rs587781985(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61780342
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781985
ebirs587781985
HLIrs587781985
Exacrs587781985
Varsomers587781985
Maprs587781985
PheGenIrs587781985
hapmaprs587781985
1000 genomesrs587781985
hgdprs587781985
ensemblrs587781985
gopubmedrs587781985
geneviewrs587781985
scholarrs587781985
googlers587781985
pharmgkbrs587781985
gwascentralrs587781985
openSNPrs587781985
23andMers587781985
23andMe allrs587781985
SNP Nexus

SNPshotrs587781985
SNPdbers587781985
MSV3drs587781985
GWAS Ctlgrs587781985
Max Magnitude0
ClinVar
Risk rs587781985(G;G)
Alt rs587781985(G;G)
Reference rs587781985(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59857703_59857704insC
CLNSRC
CLNACC RCV000130385.2,