ClinVar Miner

Submissions for variant NM_002582.4(PARN):c.1692A>G (p.Val564=)

dbSNP: rs1596433626
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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 RCV001498866 SCV001703620 likely benign Dyskeratosis congenita, autosomal recessive 6; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4 2020-11-27 criteria provided, single submitter clinical testing

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