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rs766044684

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs766044684(-;-)
Make rs766044684(-;T)
Make rs766044684(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89953437
GeneNBN
is asnp
is mentioned by
dbSNPrs766044684
ebirs766044684
HLIrs766044684
Exacrs766044684
Varsomers766044684
Maprs766044684
PheGenIrs766044684
hapmaprs766044684
1000 genomesrs766044684
hgdprs766044684
ensemblrs766044684
gopubmedrs766044684
geneviewrs766044684
scholarrs766044684
googlers766044684
pharmgkbrs766044684
gwascentralrs766044684
openSNPrs766044684
23andMers766044684
23andMe allrs766044684
SNP Nexus

SNPshotrs766044684
SNPdbers766044684
MSV3drs766044684
GWAS Ctlgrs766044684
Max Magnitude0
ClinVar
Risk rs766044684(T;T)
Alt rs766044684(T;T)
Reference rs766044684(;)
Significance 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.90965666dupT
CLNSRC
CLNACC RCV000221563.1,