NM_000212.2:c.176T>C

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HGVS Expressions

  • NG_008332.2:g.34523T>C
  • NM_000212.2:c.176T>C
  • NP_000203.2:p.Leu59Pro
  • NC_000017.11:g.47283364T>C

Associated Genes

Integrin, Beta-3
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

5918

Clinvar

13558

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
173470.G.1.1Lebanon620.19BenignSabbagh et al. 2007 205 samples from healthy Lebanese indivi...
173470.G.1.2Lebanon160.19BenignSabbagh et al. 2007 205 samples from healthy Lebanese indivi...
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Contributors

  • Sami Bizzari: 16.03.2021

Edit History

  • Sami Bizzari: 16.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.