ClinVar Miner

Submissions for variant NM_000463.3(UGT1A1):c.1075G>A (p.Asp359Asn)

gnomAD frequency: 0.00001  dbSNP: rs267599273
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001733511 SCV001984004 uncertain significance Gilbert syndrome 2020-02-02 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001810752 SCV002048829 uncertain significance not provided 2021-01-15 criteria provided, single submitter clinical testing

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