NM_001146274.1:c.552+8187T>C

HGVS Expressions

  • NG_012631.1:g.103064T>C
  • NM_001146274.1:c.552+8187T>C
  • NP_001139746.1:p.?
  • NC_000010.11:g.113048313T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.30.1United Arab Emirates2990.55AssociationType 2 Diabetes Mellitus; ObesityAl-Safar et al. 2015 272 diabetics. TCF7L2 SNP found to be as...
125853.G.30.2United Arab Emirates2300.52AssociationAl-Safar et al. 2015 216 control subjects
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