NM_000812.3:c.241-53906=

HGVS Expressions

  • NG_051831.1:g.81066=
  • NM_000812.3:c.241-53906=
  • NP_000803.2:p.?
  • NC_000004.12:g.47107343=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

1372491

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.35.1United Arab EmiratesNA0.57AssociationType 2 Diabetes MellitusAl Safar et al. 2013 Discovery GWAS group comprising 178 indi...
125853.G.35.2ArabNANAAl Safar et al. 2013 Replication sample group comprising 315 ...
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