NM_001558.3:c.1051A>G

HGVS Expressions

  • NG_016275.1:g.17565A>G
  • NM_001558.3:c.1051A>G
  • NP_001549.2:p.Arg351Gly
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Genomic Location

chr11:117998955

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

2229113

Clinvar

302554

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
266600.G.2.3Lebanon1590.72BenignInflammatory Bowel Disease 1Ghaith et al. 2010 Study of a group of 222 patients with IB...
266600.G.2.4Lebanon1580.69BenignGhaith et al. 2010 Study of a group of 230 controls
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