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rs876659592

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659592(-;-)
Make rs876659592(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89981507
GeneNBN
is asnp
is mentioned by
dbSNPrs876659592
ebirs876659592
HLIrs876659592
Exacrs876659592
Varsomers876659592
Maprs876659592
PheGenIrs876659592
hapmaprs876659592
1000 genomesrs876659592
hgdprs876659592
ensemblrs876659592
gopubmedrs876659592
geneviewrs876659592
scholarrs876659592
googlers876659592
pharmgkbrs876659592
gwascentralrs876659592
openSNPrs876659592
23andMers876659592
23andMe allrs876659592
SNP Nexus

SNPshotrs876659592
SNPdbers876659592
MSV3drs876659592
GWAS Ctlgrs876659592
Max Magnitude0
ClinVar
Risk rs876659592(;)
Alt rs876659592(;)
Reference rs876659592(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NBN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000008.10:g.90993735delA
CLNSRC
CLNACC RCV000221586.1,