ClinVar Miner

Submissions for variant NM_001003841.3(SLC6A19):c.343+37_343+75del

dbSNP: rs774243050
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002092388 SCV002324722 benign not provided 2024-12-13 criteria provided, single submitter clinical testing

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