NM_017774.3:c.371+11642G>C

HGVS Expressions

  • NG_021195.1:g.131563G>C
  • NM_017774.3:c.371+11642G>C
  • NC_000006.12:g.20661019G>C
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7754840

Clinvar

812171

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.4.1Lebanon4550.33AssociationType 2 Diabetes MellitusNemr et al, 2012a Study with 630 T2DM patients
125853.G.4.2Lebanon4470.27Nemr et al, 2012a Group consisting of 792 control subjects
125853.G.14.1Lebanon9680.31AssociationType 2 Diabetes MellitusGhassibe-Sabbagh et al. 2014 Study with 1384 T2DM patients
125853.G.14.2Lebanon10880.31Ghassibe-Sabbagh et al. 2014 Group consisting of 1902 healthy control...
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