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rs779466229

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs779466229(-;-)
Make rs779466229(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61808752
GeneBRIP1
is asnp
is mentioned by
dbSNPrs779466229
ebirs779466229
HLIrs779466229
Exacrs779466229
Varsomers779466229
Maprs779466229
PheGenIrs779466229
hapmaprs779466229
1000 genomesrs779466229
hgdprs779466229
ensemblrs779466229
gopubmedrs779466229
geneviewrs779466229
scholarrs779466229
googlers779466229
pharmgkbrs779466229
gwascentralrs779466229
openSNPrs779466229
23andMers779466229
23andMe allrs779466229
SNP Nexus

SNPshotrs779466229
SNPdbers779466229
MSV3drs779466229
GWAS Ctlgrs779466229
Max Magnitude0
ClinVar
Risk rs779466229(;)
Alt rs779466229(;)
Reference rs779466229(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.59886113delA
CLNSRC
CLNACC RCV000215252.1,