ClinVar Miner

Submissions for variant NM_001080442.3(SLC38A8):c.1162+262T>C

gnomAD frequency: 0.65876  dbSNP: rs9927180
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
GeneDx RCV001708407 SCV001934796 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001708407 SCV005248979 benign not provided criteria provided, single submitter not provided

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