NM_017774.3:c.371+24272T>C

HGVS Expressions

  • NG_021195.1:g.144193T>C
  • NM_017774.3:c.371+24272T>C
  • NC_000006.12:g.20673649T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7451008

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.14.1Lebanon0.29AssociationType 2 Diabetes MellitusGhassibe-Sabbagh et al. 2014 Study with 1384 T2DM patients
125853.G.14.2Lebanon0.29Ghassibe-Sabbagh et al. 2014 Group consisting of 1902 healthy control...
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