Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777605
rs587777605
Entrez Id: 11043;101928335
Gene Symbol: MID2;LOC101928335
MID2;LOC101928335
CUI: C3890168
Disease:
MENTAL RETARDATION, X-LINKED 101
0.800 GeneticVariation UNIPROT Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India. 24115387 2014
dbSNP: rs587777605
rs587777605
Entrez Id: 11043;101928335
Gene Symbol: MID2;LOC101928335
MID2;LOC101928335
CUI: C3890168
Disease:
MENTAL RETARDATION, X-LINKED 101
A 0.800 CausalMutation CLINVAR