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rs730881850

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881850(A;A)
Make rs730881850(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89955281
GeneNBN
is asnp
is mentioned by
dbSNPrs730881850
ebirs730881850
HLIrs730881850
Exacrs730881850
Varsomers730881850
Maprs730881850
PheGenIrs730881850
hapmaprs730881850
1000 genomesrs730881850
hgdprs730881850
ensemblrs730881850
gopubmedrs730881850
geneviewrs730881850
scholarrs730881850
googlers730881850
pharmgkbrs730881850
gwascentralrs730881850
openSNPrs730881850
23andMers730881850
23andMe allrs730881850
SNP Nexus

SNPshotrs730881850
SNPdbers730881850
MSV3drs730881850
GWAS Ctlgrs730881850
Max Magnitude0
ClinVar
Risk rs730881850(A;A)
Alt rs730881850(A;A)
Reference rs730881850(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90967509A>T
CLNSRC
CLNACC RCV000160788.1,