NM_001146274.1:c.450+29705T>C

HGVS Expressions

  • NG_012631.1:g.49080T>C
  • NM_001146274.1:c.450+29705T>C
  • NC_000010.11:g.112994329T>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7901695

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.7.1Lebanon6430.47AssociationType 2 Diabetes MellitusNemr et al, 2012c Study with 691 T2DM patients
125853.G.7.2Lebanon7090.39Nemr et al, 2012c Group consisting of 919 control subjects
125853.G.14.1Lebanon12230.41AssociationType 2 Diabetes MellitusGhassibe-Sabbagh et al. 2014 Study with 1384 T2DM patients
125853.G.14.2Lebanon14410.41Ghassibe-Sabbagh et al. 2014 Group consisting of 1902 healthy control...
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