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rs786203223

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203223(G;G)
Make rs786203223(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position89946138
GeneNBN
is asnp
is mentioned by
dbSNPrs786203223
ebirs786203223
HLIrs786203223
Exacrs786203223
Varsomers786203223
Maprs786203223
PheGenIrs786203223
hapmaprs786203223
1000 genomesrs786203223
hgdprs786203223
ensemblrs786203223
gopubmedrs786203223
geneviewrs786203223
scholarrs786203223
googlers786203223
pharmgkbrs786203223
gwascentralrs786203223
openSNPrs786203223
23andMers786203223
23andMe allrs786203223
SNP Nexus

SNPshotrs786203223
SNPdbers786203223
MSV3drs786203223
GWAS Ctlgrs786203223
Max Magnitude0
ClinVar
Risk rs786203223(G;G)
Alt rs786203223(G;G)
Reference rs786203223(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90958366A>C
CLNSRC
CLNACC RCV000166440.1,