NM_021977.3:c.429+432A>G

HGVS Expressions

  • NM_021977.3:c.429+432A>G
  • NP_068812.1:p.?
  • NC_000006.12:g.160349280A>G
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

474513

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.32.1United Arab EmiratesNA0.482AssociationType 2 Diabetes MellitusOsman et al. 2020 422 subjects with T2DM from a study cons...
125853.G.32.2United Arab EmiratesNA0.467Osman et al. 2020 Group consisting of 332 control subjects...
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