ClinVar Miner

Submissions for variant NM_015599.3(PGM3):c.39C>T (p.His13=)

gnomAD frequency: 0.00001  dbSNP: rs763886701
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000904960 SCV001049518 likely benign Immunodeficiency 23 2024-01-02 criteria provided, single submitter clinical testing

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