ASXL3, ASXL transcriptional regulator 3, 80816

N. diseases: 77; N. variants: 22
Disease: BAINBRIDGE-ROPERS SYNDROME ×
Source: CLINVAR ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568359734
rs1568359734
Entrez Id: 80816
Gene Symbol: ASXL3
ASXL3
CUI: C3809650
Disease:
BAINBRIDGE-ROPERS SYNDROME 		G 0.700 CausalMutation CLINVAR