Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781655

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781655(A;A)
Make rs587781655(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61808466
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781655
ebirs587781655
HLIrs587781655
Exacrs587781655
Varsomers587781655
Maprs587781655
PheGenIrs587781655
hapmaprs587781655
1000 genomesrs587781655
hgdprs587781655
ensemblrs587781655
gopubmedrs587781655
geneviewrs587781655
scholarrs587781655
googlers587781655
pharmgkbrs587781655
gwascentralrs587781655
openSNPrs587781655
23andMers587781655
23andMe allrs587781655
SNP Nexus

SNPshotrs587781655
SNPdbers587781655
MSV3drs587781655
GWAS Ctlgrs587781655
Max Magnitude0
ClinVar
Risk rs587781655(A;A)
Alt rs587781655(A;A)
Reference rs587781655(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59885827C>T
CLNSRC
CLNACC RCV000129793.2,