NM_000102.4:c.-34T>C

HGVS Expressions

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

chr10:102837395

Clinical Significance

Benign

Variant Type

Substitution

dbSNP

743572

Clinvar

298630

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
176807.G.1.1Lebanon64BenignProstate CancerEl Ezzi et al. 2017 69 patients with confirmed prostate cancer
176807.G.1.2Lebanon73BenignEl Ezzi et al. 2017 69 Lebanese control subjects
600082.G.1.1LebanonBenignEl Ezzi et al. 2014 68 patients with BPH. VDR SNPs (c.2T>G) ...
600082.G.1.2LebanonEl Ezzi et al. 2014 79 Lebanese controls
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