HB Dunn NM_000558.5:c.19G>A

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  2. HB Dunn NM_000558.5:c.19G>A

HGVS Expressions

  • NG_059186.1:g.5085G>A
  • HB Dunn NM_000558.5:c.19G>A
  • NP_000549.1:p.Asp7Asn
  • NC_000016.10:g.176735G>A

Associated Genes

Hemoglobin - Alpha Locus 1
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

33961916

Clinvar

15722

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613985.20MoroccoNAUncertain Significance Patient has both HB Dunn and Hb O-Arab m...
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Contributors

  • Asha Deepthi: 10.01.2021

Edit History

  • Asha Deepthi: 10.01.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.