NM_003057.3:c.1498+43=

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HGVS Expressions

  • NM_003057.3:c.1498+43=
  • NC_000006.12:g.160154953=

Associated Genes

Solute Carrier Family 22 (Organic Cation Transporter), Member 1
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Variant Type

Substitution

dbSNP

2297374

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605552.G.3.1United Arab Emirates0.435Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.529Osman et al. 2020b 104 control subjects
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Contributors

  • Pratibha Nair: 19.04.2022

Edit History

  • Pratibha Nair: 05.12.2022
  • Pratibha Nair: 26.04.2022
  • Pratibha Nair: 19.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.