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NM_182548.4:c.1A>G
Home
NM_182548.4:c.1A>G
HGVS Expressions
NG_012184.2:g.5378A>G
NM_182548.4:c.1A>G
NP_872354.1:p.Met1Val
Associated Genes
LHFP-Like Protein 5
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Genomic Location
chr6:35805671
Clinvar Clinical Significance
Pathogenic
CTGA Clinical Significance
Pathogenic
Variant Type
Substitution
dbSNP
1060499810
Clinvar
402282
Epidemiology in the Arab World
View Map
Palestine
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
610265.1.1
Palestine
2
Pathogenic
Deafness, Autosomal Recessive 67
Shahin et al. 2010
610265.1.2
Palestine
2
Pathogenic
Deafness, Autosomal Recessive 67
Shahin et al. 2010
Sister of 610265.1.1
610265.1.3
Palestine
2
Pathogenic
Deafness, Autosomal Recessive 67
Shahin et al. 2010
First cousin of 610265.1.1
610265.1.4
Palestine
2
Pathogenic
Deafness, Autosomal Recessive 67
Shahin et al. 2010
First cousin of 610265.1.1, brother of 6...
610265.1.5
Palestine
2
Pathogenic
Deafness, Autosomal Recessive 67
Shahin et al. 2010
First cousin of 610265.1.1, brother of 6...
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Contributors
Sayeeda Hana: 03.08.2020
Edit History
Sayeeda Hana: 03.08.2020
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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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