NM_000439.5:c.661A>G

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HGVS Expressions

  • NG_021161.1:g.22201A>G
  • NM_000439.5:c.661A>G
  • NP_000430.3:p.Asn221Asp
  • NC_000005.10:g.96416081T>C

Associated Genes

Proprotein Convertase, Subtilisin/Kexin-Type, 1
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Clinvar Clinical Significance

Benign, Risk factor

Variant Type

Substitution

dbSNP

6232

Clinvar

14040

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601665.G.3.1United Arab Emirates370.059ObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates460.059El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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Contributors

  • Asha Deepthi: 02.08.2021

Edit History

  • Asha Deepthi: 04.08.2021
  • Asha Deepthi: 02.08.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.