ClinVar Miner

List of variants in gene HADHB reported as likely benign for 3-hydroxyacyl-CoA dehydrogenase deficiency

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_000183.3(HADHB):c.*500G>A
NM_000183.3(HADHB):c.1098A>T (p.Ala366=) rs748353295
NM_000183.3(HADHB):c.1119T>C (p.Ile373=) rs77943157
NM_000183.3(HADHB):c.1206C>T (p.Tyr402=) rs146538551
NM_000183.3(HADHB):c.135G>A (p.Thr45=) rs574464531
NM_000183.3(HADHB):c.1371G>A (p.Ala457=) rs72851542
NM_000183.3(HADHB):c.209+7A>G rs773618132
NM_000183.3(HADHB):c.210-9G>A rs538575997
NM_000183.3(HADHB):c.246A>G (p.Ala82=) rs151302743
NM_000183.3(HADHB):c.423C>T (p.Ala141=) rs374569092
NM_000183.3(HADHB):c.64+11T>C rs57709136

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