Gene: NOD2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895467
rs104895467
NOD2
0.720 GeneticVariation UNIPROT

dbSNP: rs104895483
rs104895483
NOD2
0.710 GeneticVariation UNIPROT

dbSNP: rs3813758
rs3813758
NOD2
0.710 GeneticVariation UNIPROT

dbSNP: rs62029861
rs62029861
NOD2
0.710 GeneticVariation UNIPROT

dbSNP: rs104895428
rs104895428
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895429
rs104895429
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895431
rs104895431
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895432
rs104895432
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895438
rs104895438
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895439
rs104895439
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895440
rs104895440
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895442
rs104895442
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895443
rs104895443
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895444
rs104895444
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895445
rs104895445
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895446
rs104895446
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895447
rs104895447
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895453
rs104895453
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895468
rs104895468
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895469
rs104895469
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895470
rs104895470
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs104895471
rs104895471
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs34684955
rs34684955
NOD2
0.700 GeneticVariation UNIPROT

dbSNP: rs2066844
rs2066844
NOD2
1.000 GeneticVariation UNIPROT Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576

2001
dbSNP: rs2066845
rs2066845
NOD2
1.000 GeneticVariation UNIPROT Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576

2001