NM_000498.3:c.-344=

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HGVS Expressions

  • NG_008374.1:g.4660=
  • NM_000498.3:c.-344=
  • NC_000008.11:g.142918184=

Associated Genes

Cytochrome P450, Subfamily XIB, Polypeptide 2
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Clinvar Clinical Significance

Association

CTGA Clinical Significance

Benign

Variant Type

Reference Allele

dbSNP

1799998

Clinvar

16883

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.37.3United Arab Emirates800.65BenignType 2 Diabetes MellitusAl-Safar et al. 2013b 40 T2DM patients
125853.G.37.6United Arab Emirates780.56Al-Safar et al. 2013b 39 healthy (control) subjects
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Contributors

  • Asha Deepthi: 21.04.2022

Edit History

  • Asha Deepthi: 21.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.