ClinVar Miner

Submissions for variant NM_019023.5(PRMT7):c.1650+27A>C

dbSNP: rs1868159
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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 RCV001789599 SCV002031874 benign Short stature-brachydactyly-obesity-global developmental delay syndrome 2021-10-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710371 SCV005252729 benign not provided criteria provided, single submitter not provided

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