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rs34936594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34936594(C;G)
Make rs34936594(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50699655
GeneNOD2
is asnp
is mentioned by
dbSNPrs34936594
dbSNP (classic)rs34936594
ClinGenrs34936594
ebirs34936594
HLIrs34936594
Exacrs34936594
Gnomadrs34936594
Varsomers34936594
LitVarrs34936594
Maprs34936594
PheGenIrs34936594
Biobankrs34936594
1000 genomesrs34936594
hgdprs34936594
ensemblrs34936594
geneviewrs34936594
scholarrs34936594
googlers34936594
pharmgkbrs34936594
gwascentralrs34936594
openSNPrs34936594
23andMers34936594
23andMe allrs34936594
SNPshotrs34936594
SNPdbers34936594
MSV3drs34936594
GWAS Ctlgrs34936594
Max Magnitude0
ClinVar
Risk rs34936594(G;G)
Alt rs34936594(G;G)
Reference Rs34936594(C;C)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene NOD2
CLNDBN Behcet's syndrome
Reversed 0
HGVS NC_000016.9:g.50733566C>G
CLNSRC
CLNACC RCV000258045.1,