MID1, midline 1, 4281

N. diseases: 77; N. variants: 22
Disease: Opitz GBBB Syndrome, X-Linked ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556003095
rs1556003095
Entrez Id: 4281
Gene Symbol: MID1
MID1
CUI: C2936904
Disease:
Opitz GBBB Syndrome, X-Linked 		TATCA 0.700 CausalMutation CLINVAR