NM_014981.1:c.4797-957=

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HGVS Expressions

  • NM_014981.1:c.4797-957=
  • NP_055796.1:p.?
  • NC_000003.12:g.108400224=

Associated Genes

Myosin, Heavy Chain 15
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Variant Type

Reference Allele

dbSNP

4273371

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 Emirates0.463Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.553Osman et al. 2020b 104 control subjects
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Contributors

  • Pratibha Nair: 12.04.2022

Edit History

  • Asha Deepthi: 05.12.2022
  • Pratibha Nair: 14.04.2022
  • Pratibha Nair: 12.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.