NM_173851.3:c.973C>T

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HGVS Expressions

  • NG_016991.1:g.227272C>T
  • NM_173851.3:c.973C>T
  • NP_776250.2:p.Arg325Trp
  • NC_000008.11:g.117172544C>T

Associated Genes

Solute Carrier Family 30 (Zinc Transporter), Member 8
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

13266634

Clinvar

1000

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.6.1Lebanon0.244Type 2 Diabetes MellitusMtiraoui et al, 2012 Study with 751 Lebanese T2DM patients
125853.G.6.2Lebanon0.246Mtiraoui et al, 2012 Group consisting of 918 Lebanese control...
125853.G.6.3Tunisia0.227AssociationType 2 Diabetes MellitusMtiraoui et al, 2012 Study with 1470 Tunisian T2DM patients
125853.G.6.4Tunisia0.176AssociationMtiraoui et al, 2012 Group consisting of 838 Tunisian control...
611145.G.2Lebanon1081BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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Contributors

  • Asha Deepthi: 20.05.2020

Edit History

  • Asha Deepthi: 03.06.2021
  • Asha Deepthi: 24.05.2021
  • Sami Bizzari: 14.03.2021
  • Asha Deepthi: 21.05.2020
  • Asha Deepthi: 20.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.