NM_001290216.3:c.-280+4770=

HGVS Expressions

  • NG_029013.3:g.240624=
  • NM_001290216.3:c.-280+4770=
  • NP_001277145.1:p.?
  • NC_000003.12:g.25064946=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

6804842

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.27.1United Arab EmiratesNA0.444AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Group consisting of 464 T2DM patients. S...
125853.G.27.2United Arab EmiratesNA0.482Osman et al. 2018 Group consisting of 415 control subjects...
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