"Ambry Genetics"[submitter] AND "LOC126862407"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2543075	NM_199355.4(ADAMTS18):c.3518A>T (p.Asn1173Ile)	ADAMTS18, LOC126862407 (N1173I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2296954	NM_199355.4(ADAMTS18):c.3500C>G (p.Pro1167Arg)	ADAMTS18, LOC126862407 (P1167R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1463419	NM_199355.4(ADAMTS18):c.3499C>T (p.Pro1167Ser)	ADAMTS18, LOC126862407 (P1167S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3267026	NM_199355.4(ADAMTS18):c.3457C>G (p.Gln1153Glu)	ADAMTS18, LOC126862407 (Q981E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2543563	NM_199355.4(ADAMTS18):c.3427G>T (p.Val1143Phe)	ADAMTS18, LOC126862407 (V971F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2624305	NM_199355.4(ADAMTS18):c.3421G>A (p.Gly1141Arg)	ADAMTS18, LOC126862407 (G969R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar