NM_017777.4:c.262-27A>G

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HGVS Expressions

  • NG_013032.1:g.8336A>G
  • NM_017777.4:c.262-27A>G
  • NC_000017.11:g.58216270T>C

Associated Genes

MKS1 Gene
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

191488115

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615982.6Saudi Arabia1BenignAbu-Safieh et al. 2012 "BBS-F031-A" in the publication
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Contributors

  • Sayeeda Hana: 18.07.2022

Edit History

  • Sayeeda Hana: 01.08.2022
  • Sayeeda Hana: 18.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.