NM_182758.4:c.1962+6334T>G

HGVS Expressions

  • NG_017034.2:g.105425T>G
  • NM_182758.4:c.1962+6334T>G
  • NP_877435.3:p.?
  • NC_000015.10:g.53659238A>C
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Variant Type

Substitution

dbSNP

1031755

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.2United Arab Emirates0.117Osman et al. 2018 474 patients with T2DM
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