ClinVar Miner

Submissions for variant NM_000133.4(F9):c.1084A>G (p.Lys362Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV003484568 SCV004229125 likely pathogenic Hereditary factor IX deficiency disease 2022-11-29 criteria provided, single submitter clinical testing

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