rs1437544261, DONSON

N. diseases: 2
Disease: MUNGAN SYNDROME ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MUNGAN SYNDROME
CUI: C1969653
Disease: MUNGAN SYNDROME
0.010 GeneticVariation BEFREE Two apparently unrelated families with identical homozygous c.631C > T p.(Arg211Cys) variant had clinical features typical of Meier-Gorlin syndrome (MGS), while two siblings with compound heterozygous c.346delG p.(Asp116Ile*62) and c.1349A > G p.(Lys450Arg) variants presented with Seckel-like phenotype. 31407851 2019