NM_012407.4:c.283-176C>T

HGVS Expressions

  • NM_012407.4:c.283-176C>T
  • NP_036539.1:p.?
  • NC_000022.11:g.38067528C>T
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

880669

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
181500.G.1United Arab Emirates470.208BenignMoselhy et al. 2015 121 patients (71 males, 50 females) diag...
181500.G.2United Arab Emirates770.224BenignMoselhy et al. 2015 174 control subjects
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