ClinVar Miner

Submissions for variant NM_152424.4(AMER1):c.1873A>G (p.Thr625Ala)

gnomAD frequency: 0.00039  dbSNP: rs142654101
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
Invitae RCV000908506 SCV001053274 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
ITMI RCV000119993 SCV000084123 not provided not specified 2013-09-19 no assertion provided reference population

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