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rs864321625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321625(A;A)
Make rs864321625(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position137876041
GeneTNFAIP3
is asnp
is mentioned by
dbSNPrs864321625
dbSNP (classic)rs864321625
ClinGenrs864321625
ebirs864321625
HLIrs864321625
Exacrs864321625
Gnomadrs864321625
Varsomers864321625
LitVarrs864321625
Maprs864321625
PheGenIrs864321625
Biobankrs864321625
1000 genomesrs864321625
hgdprs864321625
ensemblrs864321625
geneviewrs864321625
scholarrs864321625
googlers864321625
pharmgkbrs864321625
gwascentralrs864321625
openSNPrs864321625
23andMers864321625
SNPshotrs864321625
SNPdbers864321625
MSV3drs864321625
GWAS Ctlgrs864321625
Max Magnitude0
ClinVar
Risk rs864321625(A;A)
Alt rs864321625(A;A)
Reference Rs864321625(T;T)
Significance Pathogenic
Disease Autoinflammatory syndrome
Variation info
Gene TNFAIP3
CLNDBN Autoinflammatory syndrome, familial, Behcet-like
Reversed 0
HGVS NC_000006.11:g.138197178T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203528.1,