NM_199168.4:c.*531G>A

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HGVS Expressions

  • NG_016861.2:g.11996G>A
  • NM_199168.4:c.*531G>A
  • NP_954637.1:p.?
  • NC_000010.11:g.44378102C>T

Associated Genes

Chemokine, CXC Motif, Ligand 12
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Clinvar Clinical Significance

Protective

CTGA Clinical Significance

Protective

Variant Type

Substitution

dbSNP

387906400

Clinvar

8762

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
609423.GUnited Arab Emirates180.35ProtectiveHuman Immunodeficiency Virus Type 1, Susceptibility ToSu et al. 2000 Healthy population of 26 individuals. Al...
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Contributors

  • Sami Bizzari: 26.04.2022

Edit History

  • Sami Bizzari: 26.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.