CYP1A1*2A Allele NG_061374.1:g.11229T>C

HGVS Expressions

  • NG_061374.1:g.11229T>C
  • CYP1A1*2A Allele NG_061374.1:g.11229T>C
  • NC_000015.10:g.74719300A>G
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CTGA Clinical Significance

Benign, Drug Response, Risk factor

Variant Type

Substitution

dbSNP

4646903

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
108330.G.1Lebanon0.026Drug ResponseOssaily and Zgheib. 2014
108330.G.2Arab0.151BenignMartínez-Labarga et al. 2019 58 healthy Arabs from Dubai, UAE
613659.G.1.1Lebanon4NARisk factorGastric CancerDarazy et al. 2011 13 patients with gastric cancer. Study i...
613659.G.1.2Lebanon6NAColorectal CancerDarazy et al. 2011 57 patients with colorectal cancer
613659.G.1.3Lebanon3NADarazy et al. 2011 Group consisting of 70 healthy control s...
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