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rs1064793210

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position89984551
GeneNBN
is asnp
is mentioned by
dbSNPrs1064793210
dbSNP (old)rs1064793210
ClinGenrs1064793210
ebirs1064793210
HLIrs1064793210
Exacrs1064793210
Gnomadrs1064793210
Varsomers1064793210
Maprs1064793210
PheGenIrs1064793210
Biobankrs1064793210
1000 genomesrs1064793210
hgdprs1064793210
ensemblrs1064793210
gopubmedrs1064793210
geneviewrs1064793210
scholarrs1064793210
googlers1064793210
pharmgkbrs1064793210
gwascentralrs1064793210
openSNPrs1064793210
23andMers1064793210
23andMe allrs1064793210
SNPshotrs1064793210
SNPdbers1064793210
MSV3drs1064793210
GWAS Ctlgrs1064793210
Max Magnitude0
ClinVar
Risk rs1064793210(-;-)
Alt rs1064793210(-;-)
Reference Rs1064793210(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90996779delA
CLNSRC
CLNACC RCV000480086.1,