SLAIN2, SLAIN motif family member 2, 57606

N. diseases: 8; N. variants: 3
Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6837335
rs6837335
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C0010346
Disease:
Crohn Disease 		G 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs6837335
rs6837335
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C0010346
Disease:
Crohn Disease 		G 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs7438704
rs7438704
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C0010346
Disease:
Crohn Disease 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015