Test Price
2,800 AED✅ Home Collection Available
SLC9A9 Gene (Autism Susceptibility, Type 16) Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited NGS processing.
- Premium Logistics: VIP mobile phlebotomy and temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic post-test interpretive counseling by a DHA-licensed consultant medical geneticist.
- Insurance & Billing: Direct billing verification via WhatsApp at +971 54 548 8731.
Key Specifications
- Price: 2,800 AED
- Turnaround Time: 3–4 Weeks
- Sample Types: Whole blood, extracted DNA, or FTA card
- Regulatory Compliance: DHA License No. 1143, ISO 9001:2015, UAE PDPL
Test Overview & Methodology
The SLC9A9 gene encodes a sodium/hydrogen exchanger protein critical for neuronal signaling. Pathogenic variants in SLC9A9 are directly linked to autism susceptibility type 16. This test uses Next Generation Sequencing (NGS) to analyze the entire coding region, detecting single‑nucleotide variants, insertions, and deletions with over 99.9% analytical sensitivity. Results are interpreted in accordance with ACMG guidelines and require correlation with clinical history and pedigree analysis.
| Feature | Our SLC9A9 NGS Test | Closest Alternative (Chromosomal Microarray) |
|---|---|---|
| Methodology | NGS – full gene analysis, includes exonic and splice‑site regions | Array‑based copy number variation only; misses point mutations |
| Diagnostic Resolution | Single‑nucleotide variants, indels, with >99.9% sensitivity | Macroscopic deletions/duplications >50 kb; limited genotyping |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Sample Options | Whole blood, extracted DNA, or FTA card | Whole blood only |
| Home Collection & VIP Service | 8 AM – 11 PM, ISO‑certified cold chain | Limited availability |
| Regulatory Compliance | DHA License (No. 1143), UAE PDPL, ISO 9001:2015 | Variable |
Physician Insight & Safety Protocols
“This SLC9A9 genetic test provides valuable information about autism susceptibility, but it must be interpreted within the full clinical context and family history. A positive finding does not equate to a diagnosis – it serves as a risk indicator for tailored early intervention. Ensure pre‑test genetic counseling addresses all implications, including the possibility of incidental findings. Our team offers detailed post‑result support to help you make informed decisions.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)
Patient Safety Advisory
Pre‑Test Requirements
- A mandatory genetic counselling session to construct a three‑generation pedigree is required before testing.
- A valid referral from a DHA‑licensed neurologist, clinical geneticist, or paediatrician is necessary.
- Legal guardian consent is mandatory for minors.
- Patients with acute psychiatric instability should be stabilised before elective testing.
Exclusion Criteria & Emergency Red Flags
Do Not Test Without Specialist Clearance
- Emergency red flags: Sudden severe behavioural regression, self‑harm ideation, new‑onset seizures, or any acute neurological change – seek immediate emergency medical evaluation. Do not wait for genetic results.
- Exclusion: Pregnant individuals (risk of incidental findings requires specialised consent).
Patient FAQ & Clinical Guidance
1. What is the SLC9A9 gene and its role in autism?
The SLC9A9 gene encodes a sodium/hydrogen exchanger protein crucial for neuronal signaling, and its pathogenic variants are directly linked to autism susceptibility type 16. This test examines the entire coding region of SLC9A9 using NGS, detecting even rare single‑nucleotide changes that may elevate the risk of autism spectrum disorder. Understanding your genotype can help your medical team design early behavioural and educational interventions tailored to your child’s needs.
2. How accurate is this genetic test for autism susceptibility?
Our NGS‑based SLC9A9 test delivers >99.9% analytical sensitivity for the targeted pathogenic variants, validated under ISO 9001:2015 accredited protocols. Accuracy is ensured through redundant sequencing depth and bioinformatic pipelines aligned with the latest ACMG guidelines. However, a negative result does not eliminate the possibility of other genetic or environmental factors contributing to autism; clinical correlation remains vital.
3. Do I need a doctor’s referral for this test in the UAE?
Yes, a valid referral from a DHA‑licensed neurologist, clinical geneticist, or paediatrician is mandatory under Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 concerning the use of ICT in health fields. This regulation ensures patients receive appropriate pre‑test genetic counselling, informed consent, and post‑test follow‑up. Our team can assist you in connecting with a qualified specialist and will verify your referral before scheduling the home collection.
UAE Regulatory & Data Privacy Adherence
Data Privacy & Security: All genetic data is handled in compliance with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent and confidentiality are paramount. Clinical safety and patient consent follow Federal Decree‑Law No. 4 of 2016 on Medical Liability. Our laboratory holds DHA Facility License No. 1143 and operates under ISO 9001:2015 quality management.
Clinical & Logistical Metadata
| Test Name | SLC9A9 Gene (Autism Susceptibility, Type 16) Genetic Test – NGS |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole blood, extracted DNA, or FTA card |
| Methodology Used | Next Generation Sequencing (NGS) – full gene analysis |
| ICD‑10‑CM Code | Z15.09 |
| LOINC Code | 81327-5 |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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