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rs876660080

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660080(-;-)
Make rs876660080(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61849250
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660080
ebirs876660080
HLIrs876660080
Exacrs876660080
Varsomers876660080
Maprs876660080
PheGenIrs876660080
hapmaprs876660080
1000 genomesrs876660080
hgdprs876660080
ensemblrs876660080
gopubmedrs876660080
geneviewrs876660080
scholarrs876660080
googlers876660080
pharmgkbrs876660080
gwascentralrs876660080
openSNPrs876660080
23andMers876660080
23andMe allrs876660080
SNP Nexus

SNPshotrs876660080
SNPdbers876660080
MSV3drs876660080
GWAS Ctlgrs876660080
Max Magnitude0
ClinVar
Risk rs876660080(;)
Alt rs876660080(;)
Reference rs876660080(C;C)
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.59926611delG
CLNSRC
CLNACC RCV000221096.1,