ClinVar Miner

List of variants in gene ACADS reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_000017.4(ACADS):c.990C>T (p.Arg330=) rs3915 0.59445
NM_000017.4(ACADS):c.321T>C (p.Arg107=) rs3914 0.51709
NM_000017.4(ACADS):c.625-99T>C rs555404 0.51701
NC_000012.12:g.120725715C>A rs2239760 0.39492
NC_000012.12:g.120725458C>T rs3021337 0.31040
NM_000017.4(ACADS):c.*21G>C rs3916 0.21460
NM_000017.4(ACADS):c.473-116T>C rs2014355 0.21375
NM_000017.4(ACADS):c.625G>A (p.Gly209Ser) rs1799958 0.20617
NM_000017.4(ACADS):c.47-177C>T rs11065230 0.10332
NC_000012.12:g.120725570T>C rs7303170 0.07643
NM_000017.4(ACADS):c.934-74C>T rs487915 0.05276
NM_000017.4(ACADS):c.*249G>A rs628909 0.04756
NC_000012.12:g.120725537G>T rs644065 0.03931
NM_000017.4(ACADS):c.511C>T (p.Arg171Trp) rs1800556 0.03280
NM_000017.4(ACADS):c.*310C>G rs116733542 0.02741
NM_000017.4(ACADS):c.*5G>A rs2229533 0.02244
NM_000017.4(ACADS):c.360C>T (p.Asn120=) rs76543640 0.01346
NM_000017.4(ACADS):c.1029+52C>T rs2071266 0.01321
NM_000017.4(ACADS):c.423G>A (p.Thr141=) rs2239686 0.00237
NM_000017.4(ACADS):c.1029+89dup rs57852948
NM_000017.4(ACADS):c.1030-41G>A rs140372512
NM_000017.4(ACADS):c.211-24C>T rs112669327
NM_000017.4(ACADS):c.473-30G>A rs117000908
NM_000017.4(ACADS):c.473-80G>C rs695950

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