NM_005141.5:c.-455G>A

HGVS Expressions

  • NG_008833.1:g.4577G>A
  • NM_005141.5:c.-455G>A
  • NC_000004.12:g.154562556G>A
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Benign, Uncertain Significance

Variant Type

Substitution

dbSNP

1800790

Clinvar

16388

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601367.3Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.5Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.21Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with arterial lesion
601367.37Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with small vessel lesion
134830.G.1.1Lebanon51BenignShammaa et al. 2008 The study involved 160 healthy individua...
134830.G.1.2Lebanon24BenignShammaa et al. 2008 The study involved 160 healthy individua...
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