NM_000492.4:c.744-33GATT[6]

HGVS Expressions

  • NG_016465.4:g.75732_75735GATT[6]
  • NM_000492.4:c.744-33GATT[6]
  • NC_000007.14:g.117536515_117536518GATT[6]
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

dbSNP

1805171

Clinvar

43579

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.G.12Lebanon12NAUncertain SignificanceCystic FibrosisFarhat et al, 2015 Patients from 7 Lebanese families. c.390...
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