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rs587780833

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780833(A;A)
Make rs587780833(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61847100
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587780833
ebirs587780833
HLIrs587780833
Exacrs587780833
Varsomers587780833
Maprs587780833
PheGenIrs587780833
hapmaprs587780833
1000 genomesrs587780833
hgdprs587780833
ensemblrs587780833
gopubmedrs587780833
geneviewrs587780833
scholarrs587780833
googlers587780833
pharmgkbrs587780833
gwascentralrs587780833
openSNPrs587780833
23andMers587780833
23andMe allrs587780833
SNP Nexus

SNPshotrs587780833
SNPdbers587780833
MSV3drs587780833
GWAS Ctlgrs587780833
Max Magnitude0
ClinVar
Risk rs587780833(A;A)
Alt rs587780833(A;A)
Reference rs587780833(G;G)
Significance Pathogenic
Disease Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59924461C>T
CLNSRC
CLNACC RCV000123363.1, RCV000160322.1, RCV000223616.1,