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
NM_000426.4:c.3174+23_3174+24insAT
Home
NM_000426.4:c.3174+23_3174+24insAT
HGVS Expressions
NG_008678.1:g.422755_422756insAT
NM_000426.4:c.3174+23_3174+24insAT
Associated Genes
Laminin, Alpha-2
Back to search Result
Genomic Location
chr6:129300895-129300896
CTGA Clinical Significance
Benign
Variant Type
Insertion
dbSNP
76978149
Epidemiology in the Arab World
View Map
All Countries
Algeria
Lebanon
Morocco
Tunisia
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
156225.G.1
Algeria
90
Benign
Siala et al. 2010
45 unrelated healthy controls
156225.G.2
Lebanon
70
Benign
Siala et al. 2010
35 healthy controls
156225.G.3
Morocco
100
Benign
Siala et al. 2010
50 unrelated healthy controls
156225.G.4
Tunisia
124
Benign
Siala et al. 2010
62 unrelated healthy controls
Download Table
Contributors
Pratibha Nair: 01.07.2020
Edit History
Rahila Mir: 07.02.2022
Sayeeda Hana: 05.10.2020
Pratibha Nair: 01.07.2020
Back to search Result
×
Algeria
Bahrain
Comoros
Country not specified
Djibouti
Egypt
Eritrea
Iraq
Jordan
Kuwait
Lebanon
Libya
Mauritania
Morocco
Oman
Palestine
Qatar
Saudi Arabia
Somalia
Sudan
Syria
Tunisia
United Arab Emirates
Yemen
Arab Countries with reported incidence
Arab Countries without reported incidence
Non-Arab Countries
© CAGS 2024. All rights reserved.