NM_001306087.2:c.588-1934_588-1931dup

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HGVS Expressions

  • NM_001306087.2:c.588-1934_588-1931dup
  • NP_001293016.1:p.?
  • NC_000014.9:g.57583366_57583369dup

Associated Genes

Solute Carrier Family 35 Member F4
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Variant Type

Indel

dbSNP

2308163

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.571Almheiri et al. 2019 500 healthy Emiratis (254 females)
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Contributors

  • Pratibha Nair: 15.03.2022

Edit History

  • Pratibha Nair: 06.12.2022
  • Pratibha Nair: 22.03.2022
  • Pratibha Nair: 15.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.