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rs746055479

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746055479(A;A)
Make rs746055479(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50712108
GeneNOD2
is asnp
is mentioned by
dbSNPrs746055479
dbSNP (classic)rs746055479
ClinGenrs746055479
ebirs746055479
HLIrs746055479
Exacrs746055479
Gnomadrs746055479
Varsomers746055479
LitVarrs746055479
Maprs746055479
PheGenIrs746055479
Biobankrs746055479
1000 genomesrs746055479
hgdprs746055479
ensemblrs746055479
geneviewrs746055479
scholarrs746055479
googlers746055479
pharmgkbrs746055479
gwascentralrs746055479
openSNPrs746055479
23andMers746055479
23andMe allrs746055479
SNPshotrs746055479
SNPdbers746055479
MSV3drs746055479
GWAS Ctlgrs746055479
Max Magnitude0
ClinVar
Risk rs746055479(A;A) rs746055479(T;T)
Alt rs746055479(A;A) rs746055479(T;T)
Reference Rs746055479(G;G)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene NOD2
CLNDBN Behcet's syndrome
Reversed 0
HGVS NC_000016.9:g.50746019G>T
CLNSRC
CLNACC RCV000258056.1,