SPART, spartin, 23111

N. diseases: 110; N. variants: 6
Disease: Pediatric failure to thrive ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730882198
rs730882198
Entrez Id: 23111
Gene Symbol: SPART
SPART
CUI: C2315100
Disease:
Pediatric failure to thrive 		GT 0.700 GeneticVariation CLINVAR