NM_015168.1:c.1440+71G>A

HGVS Expressions

  • NG_027798.1:g.37311G>A
  • NM_015168.1:c.1440+71G>A
  • NP_055983.1:p.?
  • NC_000019.10:g.47081442C>T
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Variant Type

Substitution

dbSNP

3745619

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 EmiratesNA0.361Type 2 Diabetes Mellitus; ObesityOsman et al. 2018 Group consisting of 464 T2DM patients. S...
125853.G.27.2United Arab EmiratesNA0.441Osman et al. 2018 Group consisting of 415 control subjects...
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