ASXL2, ASXL transcriptional regulator 2, 55252

N. diseases: 89; N. variants: 8
Disease: Melanocortin 4 Receptor Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886041065
rs886041065
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency 		T 0.700 CausalMutation CLINVAR