ClinVar Miner

Submissions for variant NM_022089.4(ATP13A2):c.1377C>T (p.Ile459=)

gnomAD frequency: 0.00001  dbSNP: rs1570823082
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001445347 SCV001648375 likely benign Kufor-Rakeb syndrome; Autosomal recessive spastic paraplegia type 78 2018-03-02 criteria provided, single submitter clinical testing

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