WRN

Werner syndrome RecQ like helicase
OMIM: 604611, ClinGen, DECIPHER

16 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 16 panels
Green WRN in Cataract Level 2: Ophthalmological disorders Version 0.631	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Lipodystrophy_Lipoatrophy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.42	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Mendeliome Version 1.4541	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.133	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Homologous_recombination_deficiency_WTS_UMCCR Level 2: Cancer Version 0.45	0 reviews	Unknown	Sources Literature Expert Review Green Tags umccr
Red WRN in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.417	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Expert Review Red Victorian Clinical Genetics Services Phenotypes Werner syndrome -277700
Green WRN in Monogenic Diabetes Level 2: Endocrine disorders Version 0.204 Component of the following Super Panels: Metabolic Disorders Superpanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.111	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Werner syndrome, 277700 (3)
Green WRN in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.404	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Werner syndrome MIM#277700
Green WRN in Additional findings_Paediatric Level 2: Screening Version 0.280	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Werner syndrome
Green WRN in Growth failure Version 1.99	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Werner syndrome, MIM# 277700 MONDO:0010196
Green WRN in Prepair 1000+ Level 2: Screening Version 2.15	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Werner syndrome, MIM#277700
Red WRN in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.147	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Werner syndrome MIM#277700
Green WRN in Prepair 500+ Level 2: Screening Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Mackenzie's Mission Phenotypes Werner syndrome, MIM#277700
Green WRN in Sarcoma soft tissue Level 2: Cancer Predisposition Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Expert list Phenotypes Soft tissue sarcoma, MONDO:0018078 Sarcoma, MONDO:0005089 Werner syndrome, MONDO:0010196 Werner syndrome, MIM#277700
Green WRN in Sarcoma non-soft tissue Level 2: Cancer Predisposition Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Expert list Phenotypes Sarcoma, MONDO:0005089 Werner syndrome, MONDO:0010196 Werner syndrome, MIM#277700