NM_017774.3:c.371+30101A>G

HGVS Expressions

  • NG_021195.2:g.150022A>G
  • NM_017774.3:c.371+30101A>G
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Genomic Location

chr6:20679478

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7756992

Clinvar

987

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.4.1Lebanon4180.36AssociationType 2 Diabetes MellitusNemr et al, 2012a Study with 630 T2DM patients
125853.G.4.2Lebanon4250.28Nemr et al, 2012a Group consisting of 792 control subjects
125853.G.14.1Lebanon9340.3AssociationType 2 Diabetes MellitusGhassibe-Sabbagh et al. 2014 Study with 1384 T2DM patients
125853.G.14.2Lebanon10460.3Ghassibe-Sabbagh et al. 2014 Group consisting of 1902 healthy control...
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