List of variants in gene ALAD reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000031.6(ALAD):c.1811_1812del	rs142213018	0.01239
NM_000031.6(ALAD):c.468G>A (p.Ala156=)	rs41305619	0.00348
NM_000031.6(ALAD):c.*317T>G	rs538745327	0.00245
NM_000031.6(ALAD):c.*771C>T	rs149384214	0.00230
NM_000031.6(ALAD):c.15C>T (p.Ser5=)	rs144608303	0.00195
NM_000031.6(ALAD):c.*1803A>G	rs41276803	0.00113
NM_000031.6(ALAD):c.*1473G>A	rs1062685	0.00040
NM_000031.6(ALAD):c.*1381G>A	rs140946306	0.00023
NM_000031.6(ALAD):c.692G>A (p.Arg231Gln)	rs201420740	0.00004
NM_000031.6(ALAD):c.-4C>T	rs755977870	0.00001

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