NM_001146274.1:c.552+9017G>T

HGVS Expressions

  • NG_012631.1:g.103894G>T
  • NM_001146274.1:c.552+9017G>T
  • NP_001139746.1:p.?
  • NC_000010.11:g.113049143G>T
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

Clinvar

7414

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.7.1Lebanon6610.48AssociationType 2 Diabetes MellitusNemr et al, 2012c Study with 691 T2DM patients
125853.G.7.2Lebanon6500.35Nemr et al, 2012c Group consisting of 919 control subjects
125853.G.20.1United Arab Emirates0.3944BenignKhan et al. 2021 890 Emiratis with T2DM
125853.G.20.2United Arab Emirates0.3586BenignKhan et al. 2021 686 control subjects
125853.G.29.1United Arab Emirates730.38AssociationType 2 Diabetes MellitusSaadi et al. 2008 95 Emiratis with diabetes
125853.G.29.2United Arab Emirates710.41AssociationType 2 Diabetes MellitusSaadi et al. 2008 85 Emiratis with pre-diabetes
125853.G.29.3United Arab Emirates1270.34Saadi et al. 2008 188 Emirati control subjects
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