ClinVar Miner

Submissions for variant NM_003097.6(SNRPN):c.3+10A>G

gnomAD frequency: 0.00515  dbSNP: rs112560608
Minimum review status: Collection method:
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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 RCV000372539 SCV000390120 uncertain significance Autism spectrum disorder 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000951127 SCV001097493 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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