C1850106[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1045368	NM_020223.4(FAM20C):c.458G>A (p.Gly153Asp)	FAM20C (G153D)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 720953	NM_020223.4(FAM20C):c.731C>T (p.Pro244Leu)	FAM20C (P244L)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1165383	NM_020223.4(FAM20C):c.784+19A>T	FAM20C	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 289269	NM_020223.4(FAM20C):c.1228T>A (p.Ser410Thr)	FAM20C (S410T)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 1168565	NM_020223.4(FAM20C):c.1505+20C>T	FAM20C	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 193729	NM_020223.4(FAM20C):c.1681G>A (p.Val561Met)	FAM20C (V561M)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 935951	NM_020223.4(FAM20C):c.1690A>C (p.Asn564His)	FAM20C (N564H)	Single nucleotide variant (missense variant)	Lethal osteosclerotic bone dysplasia +2 more	GUncertain significance
Select item 1168591	NM_020223.4(FAM20C):c.1740C>T (p.Ala580=)	FAM20C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1601716	NM_020223.4(FAM20C):c.1748C>T (p.Ala583Val)	FAM20C (A583V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign

ClinVar