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rs587782574

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782574(C;T)
Make rs587782574(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61743015
GeneBRIP1, LOC105371851
is asnp
is mentioned by
dbSNPrs587782574
ebirs587782574
HLIrs587782574
Exacrs587782574
Varsomers587782574
Maprs587782574
PheGenIrs587782574
hapmaprs587782574
1000 genomesrs587782574
hgdprs587782574
ensemblrs587782574
gopubmedrs587782574
geneviewrs587782574
scholarrs587782574
googlers587782574
pharmgkbrs587782574
gwascentralrs587782574
openSNPrs587782574
23andMers587782574
23andMe allrs587782574
SNP Nexus

SNPshotrs587782574
SNPdbers587782574
MSV3drs587782574
GWAS Ctlgrs587782574
Max Magnitude0
ClinVar
Risk rs587782574(T;T)
Alt rs587782574(T;T)
Reference rs587782574(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.59820376G>A
CLNSRC
CLNACC RCV000131801.2,