NM_000102.4:c.-34T>C

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  2. NM_000102.4:c.-34T>C

HGVS Expressions

  • NG_007955.1:g.5139T>C
  • NM_000102.4:c.-34T>C

Associated Genes

Cytochrome P450, Family 17, Subfamily A, Polypeptide 1
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Genomic Location

chr10:102837395

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

743572

Clinvar

298630

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
176807.G.1.1Lebanon640.46BenignProstate CancerEl Ezzi et al. 2017 69 patients with confirmed prostate canc...
176807.G.1.2Lebanon730.53BenignEl Ezzi et al. 2017 69 Lebanese control subjects
600082.G.1.1Lebanon0.43BenignEl Ezzi et al. 2014 68 patients with BPH. VDR SNPs (c.2T>G) ...
600082.G.1.2Lebanon0.57El Ezzi et al. 2014 79 Lebanese controls
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Contributors

  • Pratibha Nair: 13.08.2020

Edit History

  • Pratibha Nair: 04.05.2021
  • Pratibha Nair: 13.08.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.