ClinVar Miner

Submissions for variant NM_030912.3(TRIM8):c.167_169delinsTCT (p.Asn56_Gln57delinsIleTer)

dbSNP: rs2135973678
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001728032 SCV001976415 uncertain significance Focal segmental glomerulosclerosis and neurodevelopmental syndrome 2021-09-24 criteria provided, single submitter clinical testing

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