NM_176824.3:c.934+32A>G

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HGVS Expressions

  • NG_009111.1:g.26676A>G
  • NM_176824.3:c.934+32A>G
  • NC_000004.12:g.121848812T>C

Associated Genes

BBS7 Gene
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

6824258

Clinvar

262924

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
209900.8.2Saudi Arabia1BenignAbu-Safieh et al. 2012; Abu Safieh et al. 2010 Sibling of 209900.8.1 "BBS-F021-B" in t...
605231.2.1Saudi Arabia1BenignAbu-Safieh et al. 2012 "BBS-F019-A" in the publication
615987.4Saudi Arabia1BenignAbu-Safieh et al. 2012 "BBS-F011-A" in the publication
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Contributors

  • Sayeeda Hana: 13.07.2022

Edit History

  • Sayeeda Hana: 25.07.2022
  • Sayeeda Hana: 21.07.2022
  • Sayeeda Hana: 13.07.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.