ClinVar Miner

Submissions for variant NM_000478.6(ALPL):c.997+128A>G

gnomAD frequency: 0.76188  dbSNP: rs2275370
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 RCV001638454 SCV001850083 benign not provided 2018-08-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001638454 SCV005286170 benign not provided criteria provided, single submitter not provided

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