"Clinical Genetics, Academic Medical Center"[submitter] AND "ADAMTS18" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 725287	NM_199355.4(ADAMTS18):c.3157C>T (p.Arg1053Trp)	ADAMTS18 (R1053W +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GConflicting classifications of pathogenicity
Select item 731680	NM_199355.4(ADAMTS18):c.2508C>T (p.Pro836=)	ADAMTS18	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 778614	NM_199355.4(ADAMTS18):c.2349G>A (p.Gln783=)	ADAMTS18	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778615	NM_199355.4(ADAMTS18):c.2190C>T (p.Gly730=)	ADAMTS18	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1089403	NM_199355.4(ADAMTS18):c.1979G>A (p.Ser660Asn)	ADAMTS18 (S488N +1 more)	Single nucleotide variant (missense variant)	ADAMTS18-related condition +1 more	GLikely benign
Select item 714849	NM_199355.4(ADAMTS18):c.601G>A (p.Val201Ile)	ADAMTS18 (V201I)	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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