ClinVar Miner

Submissions for variant NM_139027.6(ADAMTS13):c.1309-20C>G

dbSNP: rs2130845090
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002181901 SCV002485098 likely benign not provided 2021-09-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500407 SCV002809213 likely benign Upshaw-Schulman syndrome 2022-03-07 criteria provided, single submitter clinical testing

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