NC_000002.12:g.634905T>C

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HGVS Expressions

  • NC_000002.12:g.634905T>C
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

6548238

Clinvar

812169

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601665.G.3.1United Arab Emirates5310.842AssociationObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates6260.804El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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Contributors

  • Asha Deepthi: 01.08.2021

Edit History

  • Asha Deepthi: 11.10.2021
  • Asha Deepthi: 04.08.2021
  • Asha Deepthi: 03.08.2021
  • Asha Deepthi: 01.08.2021
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© CAGS 2024. All rights reserved.