Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800601
rs1800601
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019