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rs786202494

From SNPedia

Orientationminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs786202494(-;-)
Make rs786202494(-;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position89981484
GeneNBN
is asnp
is mentioned by
dbSNPrs786202494
ebirs786202494
HLIrs786202494
Exacrs786202494
Varsomers786202494
Maprs786202494
PheGenIrs786202494
hapmaprs786202494
1000 genomesrs786202494
hgdprs786202494
ensemblrs786202494
gopubmedrs786202494
geneviewrs786202494
scholarrs786202494
googlers786202494
pharmgkbrs786202494
gwascentralrs786202494
openSNPrs786202494
23andMers786202494
23andMe allrs786202494
SNP Nexus

SNPshotrs786202494
SNPdbers786202494
MSV3drs786202494
GWAS Ctlgrs786202494
Max Magnitude0
ClinVar
Risk rs786202494(;)
Alt rs786202494(;)
Reference rs786202494(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90993712_90993713delTA
CLNSRC
CLNACC RCV000165335.1,