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rs864321626

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321626(C;T)
Make rs864321626(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position137877081
GeneTNFAIP3
is asnp
is mentioned by
dbSNPrs864321626
ebirs864321626
HLIrs864321626
Exacrs864321626
Varsomers864321626
Maprs864321626
PheGenIrs864321626
hapmaprs864321626
1000 genomesrs864321626
hgdprs864321626
ensemblrs864321626
gopubmedrs864321626
geneviewrs864321626
scholarrs864321626
googlers864321626
pharmgkbrs864321626
gwascentralrs864321626
openSNPrs864321626
23andMers864321626
23andMe allrs864321626
SNP Nexus

SNPshotrs864321626
SNPdbers864321626
MSV3drs864321626
GWAS Ctlgrs864321626
Max Magnitude0
ClinVar
Risk rs864321626(T;T)
Alt rs864321626(T;T)
Reference rs864321626(C;C)
Significance Pathogenic
Disease Autoinflammatory syndrome
Variation info
Gene TNFAIP3
CLNDBN Autoinflammatory syndrome, familial, Behcet-like
Reversed 0
HGVS NC_000006.11:g.138198218C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203503.2,