NM_024006.4:c.283+837T>C

HGVS Expressions

  • NG_011564.1:g.7481T>C
  • NM_024006.4:c.283+837T>C
  • NP_076869.1:p.?
  • NC_000016.10:g.31092475A>G
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Clinvar Clinical Significance

Benign, Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

2359612

Clinvar

225975

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608547.G.2.12United Arab Emirates470.53Drug ResponseCoumarin ResistanceAl-Mahayri et al. 2019 Study including 90 unrelated patients tr...
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