ClinVar Miner

Submissions for variant NM_003638.3(ITGA8):c.444+14G>A

gnomAD frequency: 0.77958  dbSNP: rs1954181
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001682216 SCV001903400 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730959 SCV001980761 benign Renal hypodysplasia/aplasia 1 2021-08-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001682216 SCV002409163 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001682216 SCV005316886 benign not provided criteria provided, single submitter not provided

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