ClinVar Miner

Submissions for variant NR_033294.2(SNORD118):n.116C>T

dbSNP: rs181334320
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002122979 SCV002410585 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002122979 SCV004010561 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing SNORD118: BS2; TMEM107: BS2
Breakthrough Genomics, Breakthrough Genomics RCV002122979 SCV005251646 benign not provided criteria provided, single submitter not provided

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