NM_000537.3:c.1059+83G>A

HGVS Expressions

  • NG_012122.1:g.15601G>A
  • NM_000537.3:c.1059+83G>A
  • NP_000528.1:p.?
  • NC_000001.11:g.204155737C>T

Associated Genes

Renin
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2368564

Clinvar

1239591

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.7.1United Arab Emirates3370.51AssociationHypertension, EssentialFrossard et al. 1998 331 hypertensives (167 males)
145500.G.7.2United Arab Emirates2030.36AssociationFrossard et al. 1998 279 hypertensives (141 males)
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