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Curations: Gene-Disease Validity Dosage Sensitivity Clinical Actionability Contact ClinGen

Knowledge Base

RAF1

Name
RAF1
HGNC ID
HGNC:9829
Cytogenetic Location
3p25.2
Haploinsufficiency
No Evidence
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RAF1 - Noonan syndrome-like disorder with loose anagen hair | MONDO:0011899

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

RAF1 - Noonan syndrome with multiple lentigines | MONDO:0007893

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

RAF1 - Costello syndrome | MONDO:0009026

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

RAF1 - cardiofaciocutaneous syndrome | MONDO:0015280

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

RAF1 - Noonan syndrome | MONDO:0018997

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

RAF1

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


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