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rs1064795816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position89943276
GeneNBN
is asnp
is mentioned by
dbSNPrs1064795816
dbSNP (old)rs1064795816
ClinGenrs1064795816
ebirs1064795816
HLIrs1064795816
Exacrs1064795816
Gnomadrs1064795816
Varsomers1064795816
Maprs1064795816
PheGenIrs1064795816
Biobankrs1064795816
1000 genomesrs1064795816
hgdprs1064795816
ensemblrs1064795816
gopubmedrs1064795816
geneviewrs1064795816
scholarrs1064795816
googlers1064795816
pharmgkbrs1064795816
gwascentralrs1064795816
openSNPrs1064795816
23andMers1064795816
23andMe allrs1064795816
SNPshotrs1064795816
SNPdbers1064795816
MSV3drs1064795816
GWAS Ctlgrs1064795816
Max Magnitude0
ClinVar
Risk rs1064795816(T;T)
Alt rs1064795816(T;T)
Reference Rs1064795816(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90955504C>A
CLNSRC
CLNACC RCV000486706.1,