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rs1064795634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ATTC;ATTC) 0 common in clinvar
Chromosome8
Position89981480
GeneNBN
is asnp
is mentioned by
dbSNPrs1064795634
dbSNP (old)rs1064795634
ClinGenrs1064795634
ebirs1064795634
HLIrs1064795634
Exacrs1064795634
Gnomadrs1064795634
Varsomers1064795634
Maprs1064795634
PheGenIrs1064795634
Biobankrs1064795634
1000 genomesrs1064795634
hgdprs1064795634
ensemblrs1064795634
gopubmedrs1064795634
geneviewrs1064795634
scholarrs1064795634
googlers1064795634
pharmgkbrs1064795634
gwascentralrs1064795634
openSNPrs1064795634
23andMers1064795634
23andMe allrs1064795634
SNPshotrs1064795634
SNPdbers1064795634
MSV3drs1064795634
GWAS Ctlgrs1064795634
Max Magnitude0
ClinVar
Risk rs1064795634(-;-)
Alt rs1064795634(-;-)
Reference Rs1064795634(ATTC;ATTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90993708_90993711delGAAT
CLNSRC
CLNACC RCV000478442.1,