ClinVar Miner

Submissions for variant NM_000463.3(UGT1A1):c.1026A>T (p.Pro342=)

gnomAD frequency: 0.00013  dbSNP: rs747062491
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734728 SCV000862892 uncertain significance not provided 2018-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000734728 SCV003483390 likely benign not provided 2024-10-27 criteria provided, single submitter clinical testing

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