NM_002075.4:c.825=

HGVS Expressions

  • NG_009100.2:g.10501=
  • NM_002075.4:c.825=
  • NP_002066.1:p.Ser275=
  • NC_000012.12:g.6845711=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

5443

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
139130.G.1.1United Arab Emirates800.61AssociationObineche et al. 2001 Study with 98 left ventricular hypertrop...
139130.G.1.2United Arab Emirates400.61AssociationObineche et al. 2001 Study with 98 LVH subjects- 40 were hete...
139130.G.1.4United Arab Emirates560.50Obineche et al. 2001 Control group of 115 subjects with no LV...
139130.G.1.5United Arab Emirates600.50Obineche et al. 2001 Control group of 115 subjects with no LV...
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