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rs752615209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752615209(C;G)
Make rs752615209(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50710956
GeneNOD2
is asnp
is mentioned by
dbSNPrs752615209
dbSNP (classic)rs752615209
ClinGenrs752615209
ebirs752615209
HLIrs752615209
Exacrs752615209
Gnomadrs752615209
Varsomers752615209
LitVarrs752615209
Maprs752615209
PheGenIrs752615209
Biobankrs752615209
1000 genomesrs752615209
hgdprs752615209
ensemblrs752615209
geneviewrs752615209
scholarrs752615209
googlers752615209
pharmgkbrs752615209
gwascentralrs752615209
openSNPrs752615209
23andMers752615209
23andMe allrs752615209
SNPshotrs752615209
SNPdbers752615209
MSV3drs752615209
GWAS Ctlgrs752615209
Max Magnitude0
ClinVar
Risk rs752615209(G;G) rs752615209(T;T)
Alt rs752615209(G;G) rs752615209(T;T)
Reference Rs752615209(C;C)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene NOD2
CLNDBN Behcet's syndrome
Reversed 0
HGVS NC_000016.9:g.50744867C>T
CLNSRC
CLNACC RCV000258859.1,