NM_000426.4:c.3174+23_3174+24insAT

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HGVS Expressions

  • NG_008678.1:g.422755_422756insAT
  • NM_000426.4:c.3174+23_3174+24insAT

Associated Genes

Laminin, Alpha-2
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Genomic Location

chr6:129300895-129300896

CTGA Clinical Significance

Benign

Variant Type

Insertion

dbSNP

76978149

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
156225.G.1Algeria90BenignSiala et al. 2010 45 unrelated healthy controls
156225.G.2Lebanon70BenignSiala et al. 2010 35 healthy controls
156225.G.3Morocco100BenignSiala et al. 2010 50 unrelated healthy controls
156225.G.4Tunisia124BenignSiala et al. 2010 62 unrelated healthy controls
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Contributors

  • Pratibha Nair: 01.07.2020

Edit History

  • Rahila Mir: 07.02.2022
  • Sayeeda Hana: 05.10.2020
  • Pratibha Nair: 01.07.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.