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rs786203662

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs786203662(C;C)
Make rs786203662(C;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position89971290
GeneNBN
is asnp
is mentioned by
dbSNPrs786203662
ebirs786203662
HLIrs786203662
Exacrs786203662
Varsomers786203662
Maprs786203662
PheGenIrs786203662
hapmaprs786203662
1000 genomesrs786203662
hgdprs786203662
ensemblrs786203662
gopubmedrs786203662
geneviewrs786203662
scholarrs786203662
googlers786203662
pharmgkbrs786203662
gwascentralrs786203662
openSNPrs786203662
23andMers786203662
23andMe allrs786203662
SNP Nexus

SNPshotrs786203662
SNPdbers786203662
MSV3drs786203662
GWAS Ctlgrs786203662
Max Magnitude0
ClinVar
Risk rs786203662(C;C)
Alt rs786203662(C;C)
Reference rs786203662(GT;GT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90983518_90983519delACinsG
CLNSRC
CLNACC RCV000167070.1,