NM_153704.5:c.507-19T>C

HGVS Expressions

  • NG_009190.1:g.15544T>C
  • NM_153704.5:c.507-19T>C

Associated Genes

Transmembrane Protein 67
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Genomic Location

chr8:93765387

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Benign, Likely Benign

Variant Type

Substitution

Clinvar

262754

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607361.1Lebanon2Benign, Likely BenignKhaddour et al. 2007
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