86 bp VNTR NM_173842.3:c.206-516ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC[2]

HGVS Expressions

  • NG_021240.1:g.17637_17722ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC[2]
  • NM_173842.3:c.206-516ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC[2]
  • NC_000002.12:g.113130529_113130614ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC[2]
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Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Benign

Variant Type

Indel

dbSNP

2234663

Clinvar

14674

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.G.11LebanonBenignFamilial Mediterranean FeverIbrahim et al. 2015 Group of 42 FMF patients carrying allele...
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