ClinVar Miner

Submissions for variant NM_022807.5(SNRPN):c.-672T>C

gnomAD frequency: 0.14308  dbSNP: rs7170796
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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 RCV000376376 SCV000390100 likely benign Autism spectrum disorder 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705305 SCV005211608 likely benign not provided criteria provided, single submitter not provided

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