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rs876660290

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660290(C;G)
Make rs876660290(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89958809
GeneNBN
is asnp
is mentioned by
dbSNPrs876660290
ebirs876660290
HLIrs876660290
Exacrs876660290
Varsomers876660290
Maprs876660290
PheGenIrs876660290
hapmaprs876660290
1000 genomesrs876660290
hgdprs876660290
ensemblrs876660290
gopubmedrs876660290
geneviewrs876660290
scholarrs876660290
googlers876660290
pharmgkbrs876660290
gwascentralrs876660290
openSNPrs876660290
23andMers876660290
23andMe allrs876660290
SNP Nexus

SNPshotrs876660290
SNPdbers876660290
MSV3drs876660290
GWAS Ctlgrs876660290
Max Magnitude0
ClinVar
Risk rs876660290(G;G)
Alt rs876660290(G;G)
Reference rs876660290(C;C)
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.90971037G>C
CLNSRC
CLNACC RCV000213986.1,