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rs876658183

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658183(-;-)
Make rs876658183(-;T)
Make rs876658183(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89984522
GeneNBN
is asnp
is mentioned by
dbSNPrs876658183
ebirs876658183
HLIrs876658183
Exacrs876658183
Varsomers876658183
Maprs876658183
PheGenIrs876658183
hapmaprs876658183
1000 genomesrs876658183
hgdprs876658183
ensemblrs876658183
gopubmedrs876658183
geneviewrs876658183
scholarrs876658183
googlers876658183
pharmgkbrs876658183
gwascentralrs876658183
openSNPrs876658183
23andMers876658183
23andMe allrs876658183
SNP Nexus

SNPshotrs876658183
SNPdbers876658183
MSV3drs876658183
GWAS Ctlgrs876658183
Max Magnitude0
ClinVar
Risk rs876658183(T;T)
Alt rs876658183(T;T)
Reference rs876658183(;)
Significance Probable-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.90996751dupA
CLNSRC
CLNACC RCV000217464.1,