Beta NM_199161.5:c.[209=;224=]

HGVS Expressions

  • NG_021330.1:g.[8052=;8067=]
  • Beta NM_199161.5:c.[209=;224=]
  • NP_954630.2:p.[Ala70=;Val75=]
  • NC_000011.10:g.[18269312=;18269327=]

Associated Genes

Serum Amyloid A1
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Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Haplotype

Clinvar

18108

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.G.7.3Jordan; Lebanon1Likely PathogenicFamilial Mediterranean FeverMedlej-Hashim et al. 2004 Group of 16 FMF patients with Amyloidosi...
249100.G.7.4Jordan; Lebanon1Likely PathogenicFamilial Mediterranean FeverMedlej-Hashim et al. 2004 Group of 15 FMF patients without Amyloid...
249100.G.7.5Jordan; Lebanon2Likely PathogenicFamilial Mediterranean FeverMedlej-Hashim et al. 2004 Group of 3 FMF patients with Amyloidosis...
249100.G.7.6Jordan; Lebanon2Likely PathogenicFamilial Mediterranean FeverMedlej-Hashim et al. 2004 Group of 11 FMF patients without Amyloid...
249100.G.7.7Jordan; Lebanon1Likely PathogenicFamilial Mediterranean FeverMedlej-Hashim et al. 2004 Group of 4 FMF patients without Amyloido...
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