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rs864321684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321684(C;G)
Make rs864321684(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position137877188
GeneTNFAIP3
is asnp
is mentioned by
dbSNPrs864321684
dbSNP (classic)rs864321684
ClinGenrs864321684
ebirs864321684
HLIrs864321684
Exacrs864321684
Gnomadrs864321684
Varsomers864321684
LitVarrs864321684
Maprs864321684
PheGenIrs864321684
Biobankrs864321684
1000 genomesrs864321684
hgdprs864321684
ensemblrs864321684
geneviewrs864321684
scholarrs864321684
googlers864321684
pharmgkbrs864321684
gwascentralrs864321684
openSNPrs864321684
23andMers864321684
SNPshotrs864321684
SNPdbers864321684
MSV3drs864321684
GWAS Ctlgrs864321684
Max Magnitude0
ClinVar
Risk rs864321684(G;G)
Alt rs864321684(G;G)
Reference Rs864321684(C;C)
Significance Pathogenic
Disease Autoinflammatory syndrome
Variation info
Gene TNFAIP3
CLNDBN Autoinflammatory syndrome, familial, Behcet-like
Reversed 0
HGVS NC_000006.11:g.138198325C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000203553.1,