NM_018256.3:c.1195-225A>G

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  2. NM_018256.3:c.1195-225A>G

HGVS Expressions

  • NM_018256.3:c.1195-225A>G
  • NP_060726.3:p.?
  • NC_000002.12:g.202881162T>C

Associated Genes

WD Repeat-Containing Protein 12
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CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

6725887

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNA0.078AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
608446.G.1LebanonBenignSaade et al. 2011 Study of 2002 Lebanese subjects to asses...
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Contributors

  • Sayeeda Hana: 24.03.2021

Edit History

  • Sayeeda Hana: 06.12.2022
  • Rahila Mir: 07.02.2022
  • Asha Deepthi: 29.09.2021
  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 24.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.