CYP2E1*6 Allele NM_000773.4:c.967+1143T>A

HGVS Expressions

  • NG_008383.1:g.12678T>A
  • NM_000773.4:c.967+1143T>A
  • NC_000010.11:g.133535040T>A
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Clinvar Clinical Significance

Association

CTGA Clinical Significance

Benign, Drug Response, Protective, Uncertain Significance

Variant Type

Substitution

dbSNP

6413432

Clinvar

16888

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.4LebanonUncertain SignificanceBreast CancerZgheib et al. 2013 Study indicated no significant statistic...
124040.G.1Lebanon0.071Drug ResponseOssaily and Zgheib. 2014
124040.G.2LebanonBenignCoronary Heart Disease, Susceptibility to, 1Zgheib et al. 2010 Among 231 patients with morbid diseases,...
607339.G.4LebanonProtectiveCoronary Heart Disease, Susceptibility to, 1Zgheib et al. 2010 Among 231 patients with morbid disease, ...
613659.G.1.1Lebanon1NAGastric CancerDarazy et al. 2011 13 patients with gastric cancer. Study i...
613659.G.1.2Lebanon2NAColorectal CancerDarazy et al. 2011 57 patients with colorectal cancer
613659.G.1.3Lebanon4NADarazy et al. 2011 Group consisting of 70 healthy control s...
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