NM_024685.4:c.-52C>T

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HGVS Expressions

  • NG_016357.1:g.5033C>T
  • NM_024685.4:c.-52C>T
  • NC_000012.12:g.76348410G>A

Associated Genes

BBS10 Gene
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

79580268

Clinvar

310502

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
600151.2.4Saudi Arabia1BenignAbu-Safieh et al. 2012; Abu Safieh et al. 2010 Sibling of 600151.2.1 "BBS-F003-D" in t...
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Contributors

  • Sayeeda Hana: 20.06.2022

Edit History

  • Sayeeda Hana: 21.07.2022
  • Sayeeda Hana: 20.06.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.