Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881839

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881839(-;-)
Make rs730881839(-;A)
Make rs730881839(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89970442
GeneNBN
is asnp
is mentioned by
dbSNPrs730881839
ebirs730881839
HLIrs730881839
Exacrs730881839
Varsomers730881839
Maprs730881839
PheGenIrs730881839
hapmaprs730881839
1000 genomesrs730881839
hgdprs730881839
ensemblrs730881839
gopubmedrs730881839
geneviewrs730881839
scholarrs730881839
googlers730881839
pharmgkbrs730881839
gwascentralrs730881839
openSNPrs730881839
23andMers730881839
23andMe allrs730881839
SNP Nexus

SNPshotrs730881839
SNPdbers730881839
MSV3drs730881839
GWAS Ctlgrs730881839
Max Magnitude0
ClinVar
Risk rs730881839(A;A)
Alt rs730881839(A;A)
Reference rs730881839(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000008.10:g.90982671dupT
CLNSRC
CLNACC RCV000160766.1, RCV000222788.1,