ClinVar Miner

Submissions for variant NM_144696.6(AXDND1):c.3032-3767T>C (rs1060775)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000263320 SCV000351489 benign Steroid-resistant nephrotic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Human Genetics Disease in Children – Taif University,Taif University RCV000210058 SCV000265977 benign Nephrotic syndrome, idiopathic, steroid-resistant 2016-01-01 no assertion criteria provided clinical testing

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