NM_001080517.3:c.3196-64G>A

HGVS Expressions

  • NG_034132.1:g.80473G>A
  • NM_001080517.3:c.3196-64G>A
  • NP_001073986.1:p.?
  • NC_000003.12:g.9473172G>A
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Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3915844

Clinvar

1282931

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605552.G.3.1United Arab Emirates0.129Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.082Osman et al. 2020b 104 control subjects
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