ClinVar Miner

List of variants reported as benign for Miller syndrome

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Total variants: 16
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HGVS dbSNP
NM_001361.5(DHODH):c.*1014C>T rs79926352
NM_001361.5(DHODH):c.*1051A>G rs2287999
NM_001361.5(DHODH):c.*1171T>C rs2287998
NM_001361.5(DHODH):c.*404G>A rs150155845
NM_001361.5(DHODH):c.*569G>A rs113365769
NM_001361.5(DHODH):c.*574G>T rs2288001
NM_001361.5(DHODH):c.*595C>T rs111810095
NM_001361.5(DHODH):c.*612T>C rs7191724
NM_001361.5(DHODH):c.*748C>T rs117655998
NM_001361.5(DHODH):c.*783A>G rs2288000
NM_001361.5(DHODH):c.1022C>T (p.Ala341Val) rs61733129
NM_001361.5(DHODH):c.19A>C (p.Lys7Gln) rs3213422
NM_001361.5(DHODH):c.457C>A (p.Leu153Ile) rs61741731
NM_001361.5(DHODH):c.573G>A (p.Ala191=) rs148523165
NM_001361.5(DHODH):c.819+10G>A rs114267707
NM_001361.5(DHODH):c.983C>T (p.Pro328Leu)

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