NG_053442.1:g.752=

HGVS Expressions

  • NG_053442.1:g.752=
  • NC_000002.12:g.59078490=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

1016287

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 EmiratesNA0.313AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Group consisting of 464 T2DM patients. S...
125853.G.27.2United Arab EmiratesNA0.371Osman et al. 2018 Group consisting of 415 control subjects...
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