NM_173560.4:c.2390C>T

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HGVS Expressions

  • NG_027699.1:g.55319C>T
  • NM_173560.4:c.2390C>T
  • NP_775831.2:p.Ser797Leu
  • NC_000006.12:g.116927531C>T

Associated Genes

Regulatory Factor X, 6
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

762356403

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.29Qatar1Uncertain SignificanceType 2 Diabetes MellitusElashi et al. 2022
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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.