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NM_000583.4:c.1296T>G
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NM_000583.4:c.1296T>G
HGVS Expressions
NG_012837.3:g.57904T>G
NM_000583.4:c.1296T>G
NP_000574.2:p.Asp432Glu
NC_000004.12:g.71752617A>C
Associated Genes
Group-Specific Component
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Clinical Significance
Benign
Variant Type
Substitution
dbSNP
7041
Clinvar
15987
Epidemiology in the Arab World
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Lebanon
Subject ID
Country of Origin
Allele Count
Clinical Significance
Condition(s)
Reference
Remarks
139200.G.1
Lebanon
Association,Uncertain Significance
Medlej-Hashim et al. 2015
Study subjects with GG genotype of rs704...
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Contributors
Asha Deepthi: 22.02.2021
Edit History
Asha Deepthi: 22.02.2021
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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
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