ClinVar Miner

List of variants reported as pathogenic for Deficiency of hydroxymethylglutaryl-CoA lyase by Counsyl

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000191.3(HMGCL):c.109G>T (p.Glu37Ter) rs763494292 0.00006
NM_000191.3(HMGCL):c.122G>A (p.Arg41Gln) rs121964997 0.00004
NM_000191.3(HMGCL):c.27del (p.Arg10fs) rs1409716731 0.00002
NM_000191.3(HMGCL):c.31C>T (p.Arg11Ter) rs1212444447 0.00001
NM_000191.3(HMGCL):c.505_506del (p.Ser169fs) rs764264834
NM_000191.3(HMGCL):c.914_915del (p.Phe305fs) rs786205431

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