ClinVar Miner

List of variants in gene ASL reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000048.4(ASL):c.646C>T (p.Leu216Phe)	rs1786698960	0.00001
NM_000048.4(ASL):c.655+5G>A	rs1472293272	0.00001

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