ClinVar Miner

Submissions for variant NM_024824.5(ZC3H14):c.1354+15A>G

dbSNP: rs2297124
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV002245257 SCV002514088 benign Intellectual disability, autosomal recessive 56 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715630 SCV005297254 benign not provided criteria provided, single submitter not provided

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