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NM_000033.4:c.1509G>A
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NM_000033.4:c.1509G>A
HGVS Expressions
NG_009022.1:g.20244G>A
NM_000033.4:c.1509G>A
NP_000024.2:p.Leu503=
NC_000023.11:g.153740112G>A
Associated Genes
ATP-Binding Cassette, Subfamily D, Member 1
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CTGA Clinical Significance
Benign
Variant Type
Substitution
Epidemiology in the Arab World
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United Arab Emirates
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
300100.G.1
United Arab Emirates
27
Benign
Frossard et al. 1995
23 heterozygous and 2 homozygous women
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Contributors
Pratibha Nair: 07.02.2018
Edit History
Sami Bizzari: 24.01.2024
Pratibha Nair: 12.10.2022
Sami Bizzari: 23.08.2022
Rahila Mir: 07.02.2022
Sayeeda Hana: 04.03.2020
Pratibha Nair: 31.12.2018
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