Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782001959
rs782001959
0.800 GeneticVariation UNIPROT Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. 23092983

2012

dbSNP: rs869320708
rs869320708
0.800 GeneticVariation UNIPROT Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. 23092983

2012

dbSNP: rs782001959
rs782001959
0.800 GeneticVariation UNIPROT Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. 21865298

2011

dbSNP: rs869320708
rs869320708
0.800 GeneticVariation UNIPROT Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. 21865298

2011