ClinVar Miner

Submissions for variant NM_001136035.4(TRMT1):c.1106+26G>C

dbSNP: rs35601737
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001838953 SCV002098802 benign Intellectual developmental disorder, autosomal recessive 68 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717864 SCV005314783 benign not provided criteria provided, single submitter not provided

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