NM_006168.3:c.155C>T

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HGVS Expressions

  • NM_006168.3:c.155C>T
  • NP_006159.2:p.Ser52Phe
  • NC_000004.12:g.84498074G>A

Associated Genes

NK6 Homeobox 1
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1720864004

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.51Qatar2Uncertain SignificanceType 2 Diabetes MellitusElashi et al. 2022 Two patients
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Contributors

  • Asha Deepthi: 09.05.2025

Edit History

  • Asha Deepthi: 22.05.2025
  • Asha Deepthi: 09.05.2025
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.