العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us
216900.G.2
Home
Subject Details
Country
Saudi Arabia
HPO Terms
Retinal dystrophy
Back to search Result
Sex
Unknown
Family History
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_001298.3:c.556C>T
4+
Achromatopsia 2
Download Table
Remarks
Family with unknown number of affected members
References
Patel et al. 2016
© CAGS 2024. All rights reserved.
