NM_001122633.2:c.4235C>A

HGVS Expressions

  • NG_008285.1:g.203099C>A
  • NM_001122633.2:c.4235C>A
  • NP_001116105.1:p.Thr1412Asn
  • NC_000002.12:g.210675783C>A
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Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1047891

Clinvar

128852

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
603933.G.1.1United Arab Emirates0.36Osman et al. 2018 145 patients with diabetic kidney diseas...
603933.G.1.2United Arab Emirates0.28Osman et al. 2018 265 patients with type 2 DM, but no kidn...
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