ClinVar Miner

Submissions for variant NM_004859.4(CLTC):c.681+2dup

dbSNP: rs1598214612
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV000845033 SCV000986869 not provided CLTC-Related Disorder no assertion provided phenotyping only Variant interpretted as Likely pathogenic and reported on 09/11/2018 by GTR ID 26957. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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