NM_020935.2:c.1670+635=

HGVS Expressions

  • NM_020935.2:c.1670+635=
  • NP_065986.2:p.?
  • NC_000002.12:g.218485029=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

492400

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.24.1United Arab EmiratesNA0.363AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 880 T2DM patients with high BMI (mean = ...
125853.G.24.2United Arab EmiratesNA0.365AssociationType 2 Diabetes Mellitus; ObesityOsman et al. 2018 Male subjects from a group of 880 T2DM p...
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