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rs587780236

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780236(-;-)
Make rs587780236(-;T)
Make rs587780236(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61743118
GeneBRIP1, LOC105371851
is asnp
is mentioned by
dbSNPrs587780236
ebirs587780236
HLIrs587780236
Exacrs587780236
Varsomers587780236
Maprs587780236
PheGenIrs587780236
hapmaprs587780236
1000 genomesrs587780236
hgdprs587780236
ensemblrs587780236
gopubmedrs587780236
geneviewrs587780236
scholarrs587780236
googlers587780236
pharmgkbrs587780236
gwascentralrs587780236
openSNPrs587780236
23andMers587780236
23andMe allrs587780236
SNP Nexus

SNPshotrs587780236
SNPdbers587780236
MSV3drs587780236
GWAS Ctlgrs587780236
Max Magnitude0
ClinVar
Risk rs587780236(T;T)
Alt rs587780236(T;T)
Reference rs587780236(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59820480dupA
CLNSRC
CLNACC RCV000116138.3,