NM_000463.2:c.-41_-40dupTA

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HGVS Expressions

  • NG_033238.1:g.4963TA[8]
  • NM_000463.2:c.-41_-40dupTA
  • NC_000002.12:g.233760235TA[8]

Associated Genes

Udp-Glycosyltransferase 1 Family, Polypeptide A1
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Clinvar Clinical Significance

Benign, Pathogenic, Uncertain Significance

CTGA Clinical Significance

Pathogenic

Variant Type

Microsatellite

dbSNP

3064744

Clinvar

12275

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143500.1United Arab Emirates2PathogenicGilbert SyndromeFathalla et al. 2021
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Contributors

  • Sami Bizzari: 31.01.2022

Edit History

  • Pratibha Nair: 12.01.2023
  • Sayeeda Hana: 07.12.2022
  • Sami Bizzari: 02.02.2022
  • Sami Bizzari: 31.01.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.