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rs777367075

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs777367075(-;-)
Make rs777367075(-;A)
Make rs777367075(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61683520
GeneBRIP1
is asnp
is mentioned by
dbSNPrs777367075
ebirs777367075
HLIrs777367075
Exacrs777367075
Varsomers777367075
Maprs777367075
PheGenIrs777367075
hapmaprs777367075
1000 genomesrs777367075
hgdprs777367075
ensemblrs777367075
gopubmedrs777367075
geneviewrs777367075
scholarrs777367075
googlers777367075
pharmgkbrs777367075
gwascentralrs777367075
openSNPrs777367075
23andMers777367075
23andMe allrs777367075
SNP Nexus

SNPshotrs777367075
SNPdbers777367075
MSV3drs777367075
GWAS Ctlgrs777367075
Max Magnitude0
ClinVar
Risk rs777367075(A;A)
Alt rs777367075(A;A)
Reference rs777367075(;)
Significance Probable-Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.59760882dupA
CLNSRC
CLNACC RCV000196468.2, RCV000216896.1,