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rs876659490

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659490(-;-)
Make rs876659490(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61808482
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876659490
ebirs876659490
HLIrs876659490
Exacrs876659490
Varsomers876659490
Maprs876659490
PheGenIrs876659490
hapmaprs876659490
1000 genomesrs876659490
hgdprs876659490
ensemblrs876659490
gopubmedrs876659490
geneviewrs876659490
scholarrs876659490
googlers876659490
pharmgkbrs876659490
gwascentralrs876659490
openSNPrs876659490
23andMers876659490
23andMe allrs876659490
SNP Nexus

SNPshotrs876659490
SNPdbers876659490
MSV3drs876659490
GWAS Ctlgrs876659490
Max Magnitude0
ClinVar
Risk rs876659490(;)
Alt rs876659490(;)
Reference rs876659490(G;G)
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.59885843delC
CLNSRC
CLNACC RCV000223526.1,