SLAIN2, SLAIN motif family member 2, 57606

N. diseases: 8; N. variants: 3
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: rs551980034
rs551980034
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs551980034
rs551980034
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C2242776
Disease:
Plexiform leiomyoma 		T 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs7438704
rs7438704
Entrez Id: 57606
Gene Symbol: SLAIN2
SLAIN2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
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