ClinVar Miner

Submissions for variant NM_006947.4(SRP72):c.610+35C>T

gnomAD frequency: 0.33008  dbSNP: rs11610
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001613770 SCV001834586 benign not provided 2018-09-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810120 SCV002057169 benign Autosomal dominant aplasia and myelodysplasia 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001613770 SCV005301942 benign not provided criteria provided, single submitter not provided

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