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NM_000410.3:c.845G>A
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NM_000410.3:c.845G>A
HGVS Expressions
NG_008720.2:g.10633G>A
NM_000410.3:c.845G>A
NP_000401.1:p.Cys282Tyr
Associated Genes
HFE Gene
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Genomic Location
chr6:26092913
Clinvar Clinical Significance
Pathogenic
CTGA Clinical Significance
Pathogenic
Variant Type
Substitution
dbSNP
1800562
Clinvar
9
Epidemiology in the Arab World
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All Countries
Morocco
Tunisia
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
114550.1.1
Morocco
1
0.5%
Pathogenic
Hepatocellular Carcinoma
Ezzikouri et al. 2008
613609.5.1
Tunisia
1
0.09%
Pathogenic
Sassi et al. 2004
1 heterozygous individual out of 570 hea...
613609.G.2.3
Morocco
3
0.9%
Pathogenic
Aguilar-Martinez et al. 2001
Group of 3 newborns with Moroccan and Al...
613609.G.3
Morocco
<0.0031
Pathogenic
Samilchuk et al. 1998
1114550.G.1.5
Morocco
3
0.7%
Pathogenic
Ezzikouri et al. 2008
Group of 3 healthy controls.
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Contributors
Sayeeda Hana: 01.06.2020
Edit History
Sayeeda Hana: 03.06.2020
Sayeeda Hana: 01.06.2020
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Algeria
Bahrain
Comoros
Country not specified
Djibouti
Egypt
Eritrea
Iraq
Jordan
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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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