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rs587782047

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782047(G;T)
Make rs587782047(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61861446
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587782047
ebirs587782047
HLIrs587782047
Exacrs587782047
Varsomers587782047
Maprs587782047
PheGenIrs587782047
hapmaprs587782047
1000 genomesrs587782047
hgdprs587782047
ensemblrs587782047
gopubmedrs587782047
geneviewrs587782047
scholarrs587782047
googlers587782047
pharmgkbrs587782047
gwascentralrs587782047
openSNPrs587782047
23andMers587782047
23andMe allrs587782047
SNP Nexus

SNPshotrs587782047
SNPdbers587782047
MSV3drs587782047
GWAS Ctlgrs587782047
Max Magnitude0
ClinVar
Risk rs587782047(T;T)
Alt rs587782047(T;T)
Reference rs587782047(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.59938807C>A
CLNSRC
CLNACC RCV000130514.2, RCV000223400.1,