Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205133
rs786205133
RLIM
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		C 0.700 GeneticVariation CLINVAR Syndromic X-linked intellectual disability segregating with a missense variant in RLIM. 25735484

2015