NC_000013.11:g.113105517_113105518insCCTATATCCT

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HGVS Expressions

  • NG_009262.1:g.4727_4728insCCTATATCCT

Associated Genes

Coagulation Factor VII
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Genomic Location

chr13:113105517-113105518

Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Uncertain Significance

Variant Type

Insertion

dbSNP

5742910

Clinvar

12079

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
227500.6Arab2NAUncertain SignificanceFactor VII DeficiencyFerraresi et al, 2020 Proband #377 in the publication
227500.7Arab1NAUncertain SignificanceFactor VII DeficiencyFerraresi et al, 2020 Proband #284 in the publication
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Contributors

  • Asha Deepthi: 08.12.2020

Edit History

  • Pratibha Nair: 10.11.2022
  • Asha Deepthi: 08.12.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.