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rs587781416

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781416(-;-)
Make rs587781416(-;A)
Make rs587781416(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61849241
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781416
ebirs587781416
HLIrs587781416
Exacrs587781416
Varsomers587781416
Maprs587781416
PheGenIrs587781416
hapmaprs587781416
1000 genomesrs587781416
hgdprs587781416
ensemblrs587781416
gopubmedrs587781416
geneviewrs587781416
scholarrs587781416
googlers587781416
pharmgkbrs587781416
gwascentralrs587781416
openSNPrs587781416
23andMers587781416
23andMe allrs587781416
SNP Nexus

SNPshotrs587781416
SNPdbers587781416
MSV3drs587781416
GWAS Ctlgrs587781416
Max Magnitude0
ClinVar
Risk rs587781416(A;A)
Alt rs587781416(A;A)
Reference rs587781416(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59926603dupT
CLNSRC
CLNACC RCV000129282.2,