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rs876659305

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876659305(-;-)
Make rs876659305(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89982837
GeneNBN
is asnp
is mentioned by
dbSNPrs876659305
ebirs876659305
HLIrs876659305
Exacrs876659305
Varsomers876659305
Maprs876659305
PheGenIrs876659305
hapmaprs876659305
1000 genomesrs876659305
hgdprs876659305
ensemblrs876659305
gopubmedrs876659305
geneviewrs876659305
scholarrs876659305
googlers876659305
pharmgkbrs876659305
gwascentralrs876659305
openSNPrs876659305
23andMers876659305
23andMe allrs876659305
SNP Nexus

SNPshotrs876659305
SNPdbers876659305
MSV3drs876659305
GWAS Ctlgrs876659305
Max Magnitude0
ClinVar
Risk rs876659305(;)
Alt rs876659305(;)
Reference rs876659305(TT;TT)
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.90995065_90995066delAA
CLNSRC
CLNACC RCV000213118.1,