RANGRF

RAN guanine nucleotide release factor
OMIM: 607954, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red RANGRF in Brugada syndrome


Level 2: Cardiovascular disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Brugada syndrome, MONDO:0015263
Tags
  • refuted

Red RANGRF in Mendeliome


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
  • Expert Review Red
  • Expert Review Red
  • ClinGen
Phenotypes
  • Brugada syndrome, MONDO:0015263
Tags
  • refuted

Red RANGRF in Additional findings_Paediatric


Level 2: Screening
Version 1.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Brugada syndrome

Red RANGRF in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Brugada syndrome