ClinVar Miner

List of variants reported as likely benign for Miller syndrome by Illumina Laboratory Services, Illumina

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001361.4(DHODH):c.-29A>G rs34270657 0.06520
NM_001361.5(DHODH):c.*868A>G rs149599098 0.00547
NM_001361.5(DHODH):c.*139C>T rs140263128 0.00282
NM_001361.5(DHODH):c.294C>T (p.Asp98=) rs61747639 0.00227
NM_001361.5(DHODH):c.72C>T (p.Phe24=) rs61753576 0.00163
NM_001361.5(DHODH):c.765C>T (p.Ile255=) rs61757214 0.00128
NM_001361.5(DHODH):c.*1088T>C rs567852382 0.00063
NM_001361.5(DHODH):c.*252C>T rs147792232 0.00025
NM_001361.5(DHODH):c.*14C>T rs370049658 0.00016
NM_001361.5(DHODH):c.*1174T>G rs148338434 0.00006

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