ClinVar Miner

Variants in gene ACADS with conflicting interpretations "likely risk allele" and "uncertain significance"

Submission 1 (likely risk allele) minimum review status: Submission 1 (likely risk allele) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_000017.4(ACADS):c.1108A>G (p.Met370Val) rs566325901 0.00009

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