NC_000018.10:g.60161902T>C

HGVS Expressions

  • NC_000018.10:g.60161902T>C

Associated Genes

RPS3A Pseudogene 49
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

6567160

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.27.1United Arab EmiratesNA0.33AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Group consisting of 464 T2DM patients. S...
125853.G.27.2United Arab EmiratesNA0.278Osman et al. 2018 Group consisting of 415 control subjects...
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