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

rs886040969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886040969(A;A)
Make rs886040969(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50712357
GeneNOD2
is asnp
is mentioned by
dbSNPrs886040969
dbSNP (classic)rs886040969
ClinGenrs886040969
ebirs886040969
HLIrs886040969
Exacrs886040969
Gnomadrs886040969
Varsomers886040969
LitVarrs886040969
Maprs886040969
PheGenIrs886040969
Biobankrs886040969
1000 genomesrs886040969
hgdprs886040969
ensemblrs886040969
geneviewrs886040969
scholarrs886040969
googlers886040969
pharmgkbrs886040969
gwascentralrs886040969
openSNPrs886040969
23andMers886040969
23andMe allrs886040969
SNPshotrs886040969
SNPdbers886040969
MSV3drs886040969
GWAS Ctlgrs886040969
Max Magnitude0
ClinVar
Risk rs886040969(A;A)
Alt rs886040969(A;A)
Reference Rs886040969(G;G)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene NOD2
CLNDBN Behcet's syndrome
Reversed 0
HGVS NC_000016.9:g.50746268G>A
CLNSRC
CLNACC RCV000258046.1,