Have questions? Visit https://www.reddit.com/r/SNPedia

rs864321683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0 common genotype
Make rs864321683(-;-)
Make rs864321683(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position137879254
GeneTNFAIP3
is asnp
is mentioned by
dbSNPrs864321683
dbSNP (classic)rs864321683
ClinGenrs864321683
ebirs864321683
HLIrs864321683
Exacrs864321683
Gnomadrs864321683
Varsomers864321683
LitVarrs864321683
Maprs864321683
PheGenIrs864321683
Biobankrs864321683
1000 genomesrs864321683
hgdprs864321683
ensemblrs864321683
geneviewrs864321683
scholarrs864321683
googlers864321683
pharmgkbrs864321683
gwascentralrs864321683
openSNPrs864321683
23andMers864321683
SNPshotrs864321683
SNPdbers864321683
MSV3drs864321683
GWAS Ctlgrs864321683
Max Magnitude0
ClinVar
Risk rs864321683(-;-)
Alt rs864321683(-;-)
Reference Rs864321683(G;G)
Significance Pathogenic
Disease Autoinflammatory syndrome
Variation info
Gene TNFAIP3
CLNDBN Autoinflammatory syndrome, familial, Behcet-like
Reversed 0
HGVS NC_000006.11:g.138200391delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203526.1,