ClinVar Miner

Submissions for variant NM_024989.4(PGAP1):c.1273-17dup

dbSNP: rs3835877
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516157 SCV001724389 benign Intellectual disability, autosomal recessive 42 2024-01-30 criteria provided, single submitter clinical testing
GeneDx RCV001655757 SCV001862838 benign not provided 2019-02-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001516157 SCV002795496 benign Intellectual disability, autosomal recessive 42 2021-09-14 criteria provided, single submitter clinical testing

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