ClinVar Miner

Submissions for variant NM_198321.4(GALNT10):c.263-138A>T

gnomAD frequency: 0.00001  dbSNP: rs59278572
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pathology and Clinical Laboratory Medicine, King Fahad Medical City RCV001261641 SCV001438936 benign not specified criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706080 SCV005226624 likely benign not provided criteria provided, single submitter not provided

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