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rs876660769

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660769(-;-)
Make rs876660769(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61847152
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660769
ebirs876660769
HLIrs876660769
Exacrs876660769
Varsomers876660769
Maprs876660769
PheGenIrs876660769
hapmaprs876660769
1000 genomesrs876660769
hgdprs876660769
ensemblrs876660769
gopubmedrs876660769
geneviewrs876660769
scholarrs876660769
googlers876660769
pharmgkbrs876660769
gwascentralrs876660769
openSNPrs876660769
23andMers876660769
23andMe allrs876660769
SNP Nexus

SNPshotrs876660769
SNPdbers876660769
MSV3drs876660769
GWAS Ctlgrs876660769
Max Magnitude0
ClinVar
Risk rs876660769(;)
Alt rs876660769(;)
Reference rs876660769(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59924513delA
CLNSRC
CLNACC RCV000217247.1,