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rs587782653

From SNPedia

Orientationminus
Geno Mag Summary
(GGTGATTAAAAACT;GGTGATTAAAAACT) 0 common in clinvar
Make rs587782653(-;-)
Make rs587782653(-;GGTGATTAAAAACT)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89946211
GeneNBN
is asnp
is mentioned by
dbSNPrs587782653
ebirs587782653
HLIrs587782653
Exacrs587782653
Varsomers587782653
Maprs587782653
PheGenIrs587782653
hapmaprs587782653
1000 genomesrs587782653
hgdprs587782653
ensemblrs587782653
gopubmedrs587782653
geneviewrs587782653
scholarrs587782653
googlers587782653
pharmgkbrs587782653
gwascentralrs587782653
openSNPrs587782653
23andMers587782653
23andMe allrs587782653
SNP Nexus

SNPshotrs587782653
SNPdbers587782653
MSV3drs587782653
GWAS Ctlgrs587782653
Max Magnitude0
ClinVar
Risk rs587782653(;)
Alt rs587782653(;)
Reference rs587782653(GGTGATTAAAAACT;GGTGATTAAAAACT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90958439_90958452delAGTTTTTAATCACC
CLNSRC
CLNACC RCV000132067.2,