rs362691, RELN

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.010 GeneticVariation BEFREE A significant association of SNP rs736707, but not for SNP rs362691, with autism in the SA population is observed. 23216241 2013