Varaico: Literature-Extracted Genetic Variants

Gene:ABCA4
Variant:p.Y603H
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ABCA4

NM_000350.3:p.Y603H

Associated Papers

Contribution of genetic test results to patient management in ophthalmology: results from a Turkish Stargardt disease cohort.

Yaylacioğlu Tuncay F et al.

Turkish Journal of Medical Sciences, 2025

18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies.

Kiel C et al.

Scientific Reports, 2024

39462066 (PubMed )
Supplement: 41598_2024_77014_MOESM2_ESM.xlsx › solved_patients

Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population.

Kadyshev VV et al.

International Journal of Molecular Sciences, 2023

38003421 (PubMed )
Supplement: ijms-24-16231-s001.zip › ijms-2667660-supplementary.xlsx › ____1

Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework.

Cornelis SS et al.

Human Mutation, 2023

40225145 (PubMed )
Supplement: 6815504.f1.zip › S1_ACMG_Categorisation.xlsx › Overview_S1

Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss Patients.

Buhler VMM et al.

Genes, 2021

The Scope of Pathogenic ABCA4 Mutations Targetable by CRISPR DNA Base Editing Systems-A Systematic Review.

Piotter E et al.

Frontiers in Genetics, 2021

35154257 (PubMed )
Supplement: DataSheet1.xlsx › 2.1_German_cohort-_raw_data

Prediction of Function in ABCA4-Related Retinopathy Using Ensemble Machine Learning.

Müller PL et al.

Journal of Clinical Medicine, 2020

32751377 (PubMed )
Supplement: jcm-09-02428-s001.zip › Supplementary_Table_S1_New.pdf

Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy.

Birtel J et al.

Scientific Reports, 2018

29555955 (PubMed )
Supplement: 41598_2018_22096_MOESM1_ESM.pdf

Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial.

Parker MA et al.

Translational Vision Science & Technology, 2016

27730010 (PubMed )
Supplement: i2164-2591-5-5-10-s01.xlsx › Sheet1
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."