NM_000131.4:c.131-394T>C

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HGVS Expressions

  • NG_009262.1:g.9506T>C
  • NM_000131.4:c.131-394T>C

Associated Genes

Coagulation Factor VII
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Genomic Location

chr13:113110296

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1745939

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
227500.8Lebanon2NAUncertain SignificanceFactor VII DeficiencyFerraresi et al, 2020 Proband #90 in the publication
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Contributors

  • Asha Deepthi: 08.12.2020

Edit History

  • Asha Deepthi: 08.12.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.