NM_015313.3:c.32+21005A>G

HGVS Expressions

  • NG_027960.1:g.26372A>G
  • NM_015313.3:c.32+21005A>G
  • NP_056128.1:p.?
  • NC_000011.10:g.120358280A>G
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4938802

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.26.1United Arab EmiratesNA0.181AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 897 T2DM patients with a mean body heigh...
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