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rs886039866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039866(C;T)
Make rs886039866(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position6333376
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs886039866
dbSNP (classic)rs886039866
ClinGenrs886039866
ebirs886039866
HLIrs886039866
Exacrs886039866
Gnomadrs886039866
Varsomers886039866
LitVarrs886039866
Maprs886039866
PheGenIrs886039866
Biobankrs886039866
1000 genomesrs886039866
hgdprs886039866
ensemblrs886039866
geneviewrs886039866
scholarrs886039866
googlers886039866
pharmgkbrs886039866
gwascentralrs886039866
openSNPrs886039866
23andMers886039866
23andMe allrs886039866
SNPshotrs886039866
SNPdbers886039866
MSV3drs886039866
GWAS Ctlgrs886039866
Max Magnitude0
ClinVar
Risk rs886039866(T;T)
Alt rs886039866(T;T)
Reference Rs886039866(C;C)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene TNFRSF1A
CLNDBN Behcet's syndrome
Reversed 1
HGVS NC_000012.11:g.6442542G>A
CLNSRC
CLNACC RCV000258049.1,