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rs864321682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321682(-;-)
Make rs864321682(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position137876032
GeneTNFAIP3
is asnp
is mentioned by
dbSNPrs864321682
dbSNP (old)rs864321682
ClinGenrs864321682
ebirs864321682
HLIrs864321682
Exacrs864321682
Gnomadrs864321682
Varsomers864321682
Maprs864321682
PheGenIrs864321682
Biobankrs864321682
1000 genomesrs864321682
hgdprs864321682
ensemblrs864321682
gopubmedrs864321682
geneviewrs864321682
scholarrs864321682
googlers864321682
pharmgkbrs864321682
gwascentralrs864321682
openSNPrs864321682
23andMers864321682
23andMe allrs864321682
SNP Nexus

SNPshotrs864321682
SNPdbers864321682
MSV3drs864321682
GWAS Ctlgrs864321682
Max Magnitude0
ClinVar
Risk rs864321682(-;-)
Alt rs864321682(-;-)
Reference Rs864321682(T;T)
Significance Pathogenic
Disease Autoinflammatory syndrome
Variation info
Gene TNFAIP3
CLNDBN Autoinflammatory syndrome, familial, Behcet-like
Reversed 0
HGVS NC_000006.11:g.138197169delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000203545.1,