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rs587782344

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782344(-;-)
Make rs587782344(-;A)
Make rs587782344(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89953538
GeneNBN
is asnp
is mentioned by
dbSNPrs587782344
ebirs587782344
HLIrs587782344
Exacrs587782344
Varsomers587782344
Maprs587782344
PheGenIrs587782344
hapmaprs587782344
1000 genomesrs587782344
hgdprs587782344
ensemblrs587782344
gopubmedrs587782344
geneviewrs587782344
scholarrs587782344
googlers587782344
pharmgkbrs587782344
gwascentralrs587782344
openSNPrs587782344
23andMers587782344
23andMe allrs587782344
SNP Nexus

SNPshotrs587782344
SNPdbers587782344
MSV3drs587782344
GWAS Ctlgrs587782344
Max Magnitude0
ClinVar
Risk rs587782344(A;A)
Alt rs587782344(A;A)
Reference rs587782344(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90965767dupT
CLNSRC
CLNACC RCV000131283.2,