ClinVar Miner

Submissions for variant NM_005763.4(AASS):c.2714G>A (p.Gly905Glu)

gnomAD frequency: 0.00026  dbSNP: rs145309509
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 RCV000892223 SCV001036085 benign not provided 2025-01-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000892223 SCV005267050 benign not provided criteria provided, single submitter not provided

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