ClinGen Knowledge Base | Clinical Genome Resource

RAF1

Name: RAF1
HGNC ID: HGNC:9829
Cytogenetic Location: 3p25.2
Haploinsufficiency: No Evidence

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ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

RAF1 - Noonan syndrome-like disorder with loose anagen hair | MONDO:0011899

Curated by	Classification	Date	Report
Gene-Disease Validity	No Reported Evidence	05/31/2018	View report

RAF1 - Noonan syndrome with multiple lentigines | MONDO:0007893

Curated by	Classification	Date	Report
Gene-Disease Validity	Limited	07/25/2018	View report

RAF1 - Costello syndrome | MONDO:0009026

Curated by	Classification	Date	Report
Gene-Disease Validity	Disputed	07/24/2018	View report

RAF1 - cardiofaciocutaneous syndrome | MONDO:0015280

Curated by	Classification	Date	Report
Gene-Disease Validity	Disputed	05/31/2018	View report

RAF1 - Noonan syndrome | MONDO:0018997

Curated by	Classification	Date	Report
Gene-Disease Validity	Definitive	07/24/2018	View report

RAF1

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	No Evidence for Haploinsufficiency	03/01/2018	View report

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