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rs756363734

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756363734(C;T)
Make rs756363734(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89943252
GeneNBN
is asnp
is mentioned by
dbSNPrs756363734
ebirs756363734
HLIrs756363734
Exacrs756363734
Varsomers756363734
Maprs756363734
PheGenIrs756363734
hapmaprs756363734
1000 genomesrs756363734
hgdprs756363734
ensemblrs756363734
gopubmedrs756363734
geneviewrs756363734
scholarrs756363734
googlers756363734
pharmgkbrs756363734
gwascentralrs756363734
openSNPrs756363734
23andMers756363734
23andMe allrs756363734
SNP Nexus

SNPshotrs756363734
SNPdbers756363734
MSV3drs756363734
GWAS Ctlgrs756363734
Max Magnitude0
ClinVar
Risk rs756363734(T;T)
Alt rs756363734(T;T)
Reference rs756363734(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NBN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000008.10:g.90955480C>A
CLNSRC
CLNACC RCV000222999.1,