NM_003057.2:c.1386-2964C>A

HGVS Expressions

  • NM_003057.2:c.1386-2964C>A
  • NC_000006.12:g.160151834C>A
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CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

622342

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.9.2Lebanon140.175Drug ResponseType 2 Diabetes MellitusNaja et al, 2020b Study with 63 unrelated T2DM patients
125853.G.9.3Lebanon90NADrug ResponseType 2 Diabetes MellitusNaja et al, 2020b Study with 63 unrelated T2DM patients
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