Disease: Short middle phalanx of finger ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759103701
rs759103701
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C1846950
Disease:
Short middle phalanx of finger 		T 0.700 CausalMutation CLINVAR MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome. 15821734 2005