ClinVar Miner

Submissions for variant NM_019023.5(PRMT7):c.1905C>T (p.Pro635=)

gnomAD frequency: 0.06161  dbSNP: rs61733486
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001789600 SCV002031877 benign Short stature-brachydactyly-obesity-global developmental delay syndrome 2021-10-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074116 SCV002442357 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002074116 SCV005252773 benign not provided criteria provided, single submitter not provided

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