ClinVar Miner

Submissions for variant NM_001361.5(DHODH):c.605G>A (p.Gly202Asp)

gnomAD frequency: 0.00004  dbSNP: rs267606767
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000018296 SCV000038575 pathogenic Miller syndrome 2010-01-01 no assertion criteria provided literature only

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