ClinVar Miner

Submissions for variant NM_003097.6(SNRPN):c.-39G>A

gnomAD frequency: 0.01903  dbSNP: rs75184959
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000262201 SCV000390118 likely benign Autism spectrum disorder 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705306 SCV005211611 likely benign not provided criteria provided, single submitter not provided

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