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NM_020822.3:c.2178C>A
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NM_020822.3:c.2178C>A
HGVS Expressions
NG_033070.2:g.75700C>A
NM_020822.3:c.2178C>A
NP_065873.2:p.Asp726Glu
NC_000009.12:g.135772884C>A
Associated Genes
Potassium Channel, Subfamily T, Member 1
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CTGA Clinical Significance
Uncertain Significance
Variant Type
Substitution
dbSNP
2490988828
Epidemiology in the Arab World
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Saudi Arabia
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Subject ID
Country of Origin
Allele Count
CTGA Clinical Significance
Condition(s)
Reference
Remarks
614959.1
Saudi Arabia
1
Uncertain Significance
Developmental and Epileptic Encephalopathy 14
Monies et al. 2017
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Contributors
Asha Deepthi: 17.03.2025
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Asha Deepthi: 17.03.2025
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العربية
About Us
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العربية
Home
About Us
CTGA Database
CTGA Overview
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Genetics Made Easy
Genetic Disorders in the Arab World
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Gallery
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