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rs587781305

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781305(-;-)
Make rs587781305(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89981389
GeneNBN
is asnp
is mentioned by
dbSNPrs587781305
ebirs587781305
HLIrs587781305
Exacrs587781305
Varsomers587781305
Maprs587781305
PheGenIrs587781305
hapmaprs587781305
1000 genomesrs587781305
hgdprs587781305
ensemblrs587781305
gopubmedrs587781305
geneviewrs587781305
scholarrs587781305
googlers587781305
pharmgkbrs587781305
gwascentralrs587781305
openSNPrs587781305
23andMers587781305
23andMe allrs587781305
SNP Nexus

SNPshotrs587781305
SNPdbers587781305
MSV3drs587781305
GWAS Ctlgrs587781305
Max Magnitude0
ClinVar
Risk rs587781305(;)
Alt rs587781305(;)
Reference rs587781305(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90993617delA
CLNSRC
CLNACC RCV000129019.2,