NM_000024.5:c.46A>G

HGVS Expressions

  • NG_016421.2:g.5285A>G
  • NM_000024.5:c.46A>G
  • NP_000015.1:p.Arg16Gly
  • NC_000005.10:g.148826877=
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Clinvar Clinical Significance

Benign, Risk factor

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1042713

Clinvar

17742

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.1.1Lebanon1710.64Uncertain SignificanceHypertension, EssentialSoudani et al. 2014 Study with 134 hypertensive patients. Su...
145500.G.1.2Lebanon1160.62Soudani et al. 2014 Group consisting of 94 non-hypertensive ...
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