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rs786203920

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203920(A;T)
Make rs786203920(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position89946154
GeneNBN
is asnp
is mentioned by
dbSNPrs786203920
ebirs786203920
HLIrs786203920
Exacrs786203920
Varsomers786203920
Maprs786203920
PheGenIrs786203920
hapmaprs786203920
1000 genomesrs786203920
hgdprs786203920
ensemblrs786203920
gopubmedrs786203920
geneviewrs786203920
scholarrs786203920
googlers786203920
pharmgkbrs786203920
gwascentralrs786203920
openSNPrs786203920
23andMers786203920
23andMe allrs786203920
SNP Nexus

SNPshotrs786203920
SNPdbers786203920
MSV3drs786203920
GWAS Ctlgrs786203920
Max Magnitude0
ClinVar
Risk rs786203920(T;T)
Alt rs786203920(T;T)
Reference rs786203920(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90958382T>A
CLNSRC
CLNACC RCV000167435.1,