NM_015967.7:c.1858=

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HGVS Expressions

  • NM_015967.7:c.1858=
  • NP_057051.3:p.Arg620Trp
  • NC_000001.11:g.113834946A>G

Associated Genes

Protein Tyrosine Phosphatase, Nonreceptor-Type, 22
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

2476601

Clinvar

8909

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
222100.G.5.1United Arab Emirates150.054AssociationType 1 Diabetes MellitusSharma et al. 2021 139 patients with Type I diabetes. Signi...
222100.G.5.2United Arab Emirates30.009Sharma et al. 2021 171 healthy controls
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Contributors

  • Pratibha Nair: 08.02.2022

Edit History

  • Sami Bizzari: 13.01.2023
  • Sayeeda Hana: 06.12.2022
  • Pratibha Nair: 08.02.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.