NM_002973.4:c.252-14033G>C

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HGVS Expressions

  • NG_011572.3:g.34725G>C
  • NM_002973.4:c.252-14033G>C
  • NC_000012.12:g.111569952C>G

Associated Genes

SH2B Adaptor Protein 3
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

653178

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608446.G.1LebanonBenignSaade et al. 2011 Study of 2002 Lebanese subjects to asses...
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Contributors

  • Sayeeda Hana: 24.03.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 24.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.