ClinVar Miner

Submissions for variant NM_000382.3(ALDH3A2):c.471+31T>C

gnomAD frequency: 0.25856  dbSNP: rs1004491
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001542814 SCV001761192 benign Sjögren-Larsson syndrome 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001712990 SCV001944477 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001712990 SCV005248698 benign not provided criteria provided, single submitter not provided

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