Have questions? Visit https://www.reddit.com/r/SNPedia

rs876661189

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661189(-;-)
Make rs876661189(-;TT)
Make rs876661189(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89943327
GeneNBN
is asnp
is mentioned by
dbSNPrs876661189
ebirs876661189
HLIrs876661189
Exacrs876661189
Varsomers876661189
Maprs876661189
PheGenIrs876661189
hapmaprs876661189
1000 genomesrs876661189
hgdprs876661189
ensemblrs876661189
gopubmedrs876661189
geneviewrs876661189
scholarrs876661189
googlers876661189
pharmgkbrs876661189
gwascentralrs876661189
openSNPrs876661189
23andMers876661189
23andMe allrs876661189
SNP Nexus

SNPshotrs876661189
SNPdbers876661189
MSV3drs876661189
GWAS Ctlgrs876661189
Max Magnitude0
ClinVar
Risk rs876661189(TT;TT)
Alt rs876661189(TT;TT)
Reference rs876661189(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90955556_90955557dupAA
CLNSRC
CLNACC RCV000220883.1,