ClinVar Miner

Submissions for variant NM_004944.4(DNASE1L3):c.320+17C>A

gnomAD frequency: 0.00001  dbSNP: rs376951611
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002210755 SCV002491691 likely benign not provided 2021-10-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500440 SCV002808240 likely benign Autosomal systemic lupus erythematosus type 16 2022-01-21 criteria provided, single submitter clinical testing

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