Oculocutaneous albinism, Type 1, 2, 3, 4, 6, 7, NGS … see more Oculocutaneous albinism, Type 1, 2, 3, 4, 6, 7, NGS panel  see less
GTR Test Accession: Help GTR000521248.2
Last updated in GTR: 2016-01-26
Last annual review date for the lab: 2022-01-21 Past due LinkOut
At a Glance
Oculocutaneous albinism; Oculocutaneous albinism type 1; Oculocutaneous albinism type 3 more...
Genes (6): Help
LRMDA (10q22.2-22.3); OCA2 (15q12-13.1); SLC24A5 (15q21.1); SLC45A2 (5p13.2); TYR (11q14.3) more...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
Department of Clinical Genetics
View lab's website
View lab's test page
Test short name: Help
Specimen Source: Help
Who can order: Help
  • Genetic Counselor
  • Health Care Provider
  • Licensed Dentist
  • Licensed Physician
  • Nurse Practitioner
  • Physician Assistant
  • Public Health Mandate
  • Registered Nurse
Lab contact: Help
Contact Policy: Help
Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
How to Order: Help
A completed referral note, or a letter stating name, dob, referral reason and the test that are requested. Also an address where to send the report and the invoice.
Order URL
Test service: Help
Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Custom Deletion/Duplication Testing
Custom Sequence Analysis
Test additional service: Help
Custom mutation-specific/Carrier testing
Test development: Help
Test developed by laboratory (no manufacturer test name)
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 7
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 6
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Total methods: 1
Method Category Help
Test method Help
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Illumina MiSeq
Clinical Information
Test purpose: Help
Variant Interpretation:
What is the protocol for interpreting a variation as a VUS? Help
Missense and silent changes that are unknown to HGMD database and to SNP databases (SNP137, 1000 genomes)

Are family members with defined clinical status recruited to assess significance of VUS without charge? Help

Will the lab re-contact the ordering physician if variant interpretation changes? Help
Recommended fields not provided:
Technical Information
Test Confirmation: Help
Variations that are classified as pathogenic, probalbly pathogenic and variants of uncertain clinical significance are verified by Sanger sequencing
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
In house validation of the method has shown a sensitivity of 100 % (95% confidensinterval 95-100%) for regions with a sequencing depth of >X100.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
Software used to interpret novel variations Help
Variants are analysed using SIFT, polyphen2, Align GVGD and MutationTaster for predictions. If possible we perform segregation analysis.

Laboratory's policy on reporting novel variations Help
The person who ordered the test will receive a written report by ordinary mail.
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Category: FDA exercises enforcement discretion
Additional Information

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.