NM_000662.7:c.*215A=

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HGVS Expressions

  • NG_012245.2:g.57674A=
  • NM_000662.7:c.*215A=
  • NC_000008.11:g.18223135A=

Associated Genes

N-Acetyltransferase 1
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Reference Allele

dbSNP

1057126

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
108345.G.1Lebanon4Uncertain SignificanceDhaini and Levy. 2000 42 subjects of Lebanese origin
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Contributors

  • Pratibha Nair: 16.05.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Pratibha Nair: 16.05.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.