ClinVar Miner

Submissions for variant NM_000143.4(FH):c.1243A>G (p.Asn415Asp)

dbSNP: rs1659748903
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center of Medical Genetics and Primary Health Care RCV001269356 SCV001448703 uncertain significance Malignant tumor of breast no assertion criteria provided clinical testing

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