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rs587782065

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782065(-;-)
Make rs587782065(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61859860
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587782065
ebirs587782065
HLIrs587782065
Exacrs587782065
Varsomers587782065
Maprs587782065
PheGenIrs587782065
hapmaprs587782065
1000 genomesrs587782065
hgdprs587782065
ensemblrs587782065
gopubmedrs587782065
geneviewrs587782065
scholarrs587782065
googlers587782065
pharmgkbrs587782065
gwascentralrs587782065
openSNPrs587782065
23andMers587782065
23andMe allrs587782065
SNP Nexus

SNPshotrs587782065
SNPdbers587782065
MSV3drs587782065
GWAS Ctlgrs587782065
Max Magnitude0
ClinVar
Risk rs587782065(;)
Alt rs587782065(;)
Reference rs587782065(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59937221delG
CLNSRC
CLNACC RCV000130549.2,