NM_004774.3:c.1297+1248=

HGVS Expressions

  • NG_046996.1:g.37812=
  • NM_004774.3:c.1297+1248=
  • NP_004765.2:p.?
  • NC_000017.11:g.39418469=
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Variant Type

Reference Allele

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.3United Arab Emirates0.281Osman et al. 2018 395 patients with T2DM
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