ClinVar Miner

Submissions for variant NM_019076.5(UGT1A8):c.855+63319T>G

gnomAD frequency: 0.34319  dbSNP: rs7586110
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001707715 SCV000605524 uncertain significance not provided 2022-09-13 criteria provided, single submitter clinical testing
GeneDx RCV001707715 SCV001936111 benign not provided 2018-07-09 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 26202972, 15716465)

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