"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "LOC106050102"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 198405	NM_000202.8(IDS):c.925A>G (p.Thr309Ala)	IDS, LOC106050102 (T309A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 558995	NM_000202.8(IDS):c.709-671dup	IDS, LOC106050102	Duplication (intron variant)	not provided	GLikely benign
Select item 558996	NM_000202.8(IDS):c.709-680C>T	IDS, LOC106050102	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 457346	NM_000202.8(IDS):c.467C>A (p.Pro156Gln)	IDS, LOC106050102 (P156Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 457354	NM_000202.8(IDS):c.465T>A (p.Phe155Leu)	IDS, LOC106050102 (F155L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign
Select item 92619	NM_000202.8(IDS):c.438C>T (p.Thr146=)	IDS, LOC106050102	Single nucleotide variant (synonymous variant +1 more)	Mucopolysaccharidosis, MPS-II +3 more	GBenign
Select item 558997	NM_000202.8(IDS):c.419-6del	IDS, LOC106050102	Deletion (intron variant)	Mucopolysaccharidosis, MPS-II +1 more	GBenign/Likely benign

ClinVar