NC_000013.11:g.113113080A>G

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  2. NC_000013.11:g.113113080A>G

HGVS Expressions

  • NG_009262.1:g.12290A>G

Associated Genes

Coagulation Factor VII
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Genomic Location

chr13:113113080

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

12431329

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
227500.9Tunisia2NAUncertain SignificanceFactor VII DeficiencyFerraresi et al, 2020 Proband #15 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.