ClinVar Miner

Submissions for variant NM_015570.4(AUTS2):c.1827G>A (p.Pro609=)

gnomAD frequency: 0.00022  dbSNP: rs146043752
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 RCV000922843 SCV001068289 benign not provided 2023-11-01 criteria provided, single submitter clinical testing
GeneDx RCV000922843 SCV001771440 likely benign not provided 2021-04-28 criteria provided, single submitter clinical testing

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