Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs750612085
rs750612085
Entrez Id: 84894;105370906
Gene Symbol: LINGO1;LOC105370906
LINGO1;LOC105370906
CUI: C4748192
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
0.800 GeneticVariation UNIPROT Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. 28837161 2018
dbSNP: rs750612085
rs750612085
Entrez Id: 84894;105370906
Gene Symbol: LINGO1;LOC105370906
LINGO1;LOC105370906
CUI: C4748192
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
C 0.800 CausalMutation CLINVAR