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

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