ClinVar Miner

Submissions for variant NM_003638.3(ITGA8):c.2803G>A (p.Ala935Thr)

gnomAD frequency: 0.00722  dbSNP: rs77037561
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000962397 SCV001109475 benign not provided 2025-01-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489365 SCV002801960 likely benign Renal hypodysplasia/aplasia 1 2021-08-17 criteria provided, single submitter clinical testing

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