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rs876660613

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660613(-;-)
Make rs876660613(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61861494
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876660613
ebirs876660613
HLIrs876660613
Exacrs876660613
Varsomers876660613
Maprs876660613
PheGenIrs876660613
hapmaprs876660613
1000 genomesrs876660613
hgdprs876660613
ensemblrs876660613
gopubmedrs876660613
geneviewrs876660613
scholarrs876660613
googlers876660613
pharmgkbrs876660613
gwascentralrs876660613
openSNPrs876660613
23andMers876660613
23andMe allrs876660613
SNP Nexus

SNPshotrs876660613
SNPdbers876660613
MSV3drs876660613
GWAS Ctlgrs876660613
Max Magnitude0
ClinVar
Risk rs876660613(;)
Alt rs876660613(;)
Reference rs876660613(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.59938855delA
CLNSRC
CLNACC RCV000214696.1,