ClinVar Miner

Submissions for variant NM_032575.3(GLIS2):c.775+20C>T

gnomAD frequency: 0.00297  dbSNP: rs116598071
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246525 SCV000314982 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058376 SCV002352155 benign Nephronophthisis 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500924 SCV002805471 benign Nephronophthisis 7 2021-07-27 criteria provided, single submitter clinical testing

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