ClinVar Miner

Submissions for variant NM_006947.4(SRP72):c.*637TA[11]

dbSNP: rs35852754
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000353198 SCV000450195 uncertain significance Autosomal dominant aplasia and myelodysplasia 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003430892 SCV004152711 benign not provided 2022-08-01 criteria provided, single submitter clinical testing SRP72: BS1, BS2

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