NR_046174.2:n.873-7087=

HGVS Expressions

  • NC_000018.10:g.42567706=

Associated Genes

LINC00907
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

7239883

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.24.1United Arab EmiratesNA0.442AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 880 T2DM patients with high BMI (mean = ...
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