ClinVar Miner

Submissions for variant NM_004171.4(SLC1A2):c.1092-6T>C

dbSNP: rs2134719255
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002246841 SCV002516662 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005095833 SCV005783036 likely benign not provided 2024-05-12 criteria provided, single submitter clinical testing

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