Disease: Autistic Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1858830
rs1858830
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0004352
Disease:
Autistic Disorder 		0.030 GeneticVariation BEFREE We further described enriched association of the MET promoter variant rs1858830 C allele in families with co-occurring autism and gastrointestinal conditions. 19548256 2010
dbSNP: rs1858830
rs1858830
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0004352
Disease:
Autistic Disorder 		0.030 GeneticVariation BEFREE An interesting observation is that all three SNPs of MET (rs1858830, rs38845 and rs38841) shown to be associated with autism in three independent studies including the present one, are located towards the 5'end of the gene at a span of 9.4 kb. 20615438 2010
dbSNP: rs1858830
rs1858830
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0004352
Disease:
Autistic Disorder 		0.030 GeneticVariation BEFREE This study is the third independent study to find the rs1858830 C variant in the MET gene promoter to be associated with autism. 19681062 2009
dbSNP: rs38841
rs38841
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Association of rs38841 with autism was further confirmed in 252 Caucasian trios from AGRE (p=0.0006). 20615438 2010
dbSNP: rs38845
rs38845
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE An interesting observation is that all three SNPs of MET (rs1858830, rs38845 and rs38841) shown to be associated with autism in three independent studies including the present one, are located towards the 5'end of the gene at a span of 9.4 kb. 20615438 2010