NM_032784.5:c.567G>A

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  2. NM_032784.5:c.567G>A

HGVS Expressions

  • NM_032784.5:c.567G>A
  • NP_116173.2:p.Leu189=
  • NC_000006.12:g.127155371G>A

Associated Genes

R-Spondin 3
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Variant Type

Substitution

dbSNP

1892172

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.1United Arab Emirates0.469Osman et al. 2018 450 patients with T2DM
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Contributors

  • Pratibha Nair: 23.05.2022

Edit History

  • Pratibha Nair: 31.05.2022
  • Pratibha Nair: 23.05.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.