ClinVar Miner

Submissions for variant NM_032208.3(ANTXR1):c.1434+45_1434+46insTCAC

dbSNP: rs57847359
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
GeneDx RCV001689044 SCV001913792 benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260352 SCV002539304 benign GAPO syndrome 2021-12-05 criteria provided, single submitter clinical testing

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