NM_000795.4:c.811-83G>T

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  2. NM_000795.4:c.811-83G>T

HGVS Expressions

  • NG_008841.1:g.67314G>T
  • NM_000795.4:c.811-83G>T
  • NP_000786.1:p.?
  • NC_000011.10:g.113412966C>A

Associated Genes

Dopamine Receptor D2
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Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

1076560

Clinvar

375655

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606581.G.1.1United Arab Emirates590.12Likely BenignAlblooshi et al. 2018; Alblooshi et al. 2019 250 subjects reported with mixed substan...
606581.G.1.2United Arab Emirates690.13Alblooshi et al. 2018; Alblooshi et al. 2019 262 control subjects. No association was...
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Contributors

  • Sami Bizzari: 26.07.2022

Edit History

  • Sami Bizzari: 27.07.2022
  • Sami Bizzari: 26.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.