NM_001145795.1:c.1450A>G

HGVS Expressions

  • NG_029706.2:g.30321A>G
  • NM_001145795.1:c.1450A>G
  • NP_001139267.1:p.Thr484Ala
  • NC_000016.10:g.28871920A>G

Associated Genes

Sh2b Adaptor Protein 1
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Variant Type

Substitution

dbSNP

7498665

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601665.G.3.1United Arab Emirates1190.191ObesityEl Hajj Chehadeh et al. 2020 Study with 318 overweight/obese subjects...
601665.G.3.2United Arab Emirates1460.187El Hajj Chehadeh et al. 2020 Control group consisting of 392 subjects...
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