NM_000595.4:c.179C>A

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HGVS Expressions

  • NG_012010.1:g.5909C>A
  • NM_000595.4:c.179C>A
  • NP_000586.2:p.Thr60Asn
  • NC_000006.12:g.31573007C>A

Associated Genes

Lymphotoxin-Alpha
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1041981

Clinvar

14379

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: 23.03.2021

Edit History

  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 23.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.