ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.1569A>G (p.Ala523=)

dbSNP: rs1555612830
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000632590 SCV000753775 likely benign Neurofibromatosis, type 1 2023-09-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004586844 SCV005076391 likely benign not specified 2024-04-30 criteria provided, single submitter clinical testing

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