NC_000011.10:g.44258540C>T

HGVS Expressions

  • NC_000011.10:g.44258540C>T
  • NC_000011.10:g.44258540C>T

Associated Genes

Aristaless Homeobox 4
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

729287

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.17.1Lebanon416AssociationType 2 Diabetes MellitusAlmawi et al. 2013 Study with 995 T2DM patients. 416/1574 a...
125853.G.17.2Lebanon388AssociationAlmawi et al. 2013 Study with 1076 controls. 388/2002 allel...
125853.G.18.2Lebanon201AssociationAlmawi et al. 2013 Study with 1076 controls. 201/1297 allel...
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