"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RPS7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 335900	NM_001011.4(RPS7):c.-19+13C>T	RPS7	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 8	GBenign/Likely benign
Select item 1622041	NM_001011.4(RPS7):c.63C>T (p.Ser21=)	RPS7	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia +1 more	GLikely benign
Select item 335903	NM_001011.4(RPS7):c.75+13C>T	RPS7	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 8	GLikely benign
Select item 1401513	NM_001011.4(RPS7):c.77C>T (p.Ala26Val)	RPS7 (A26V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 701730	NM_001011.4(RPS7):c.102G>A (p.Ser34=)	RPS7	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia +1 more	GLikely benign
Select item 962784	NM_001011.4(RPS7):c.133A>G (p.Ile45Val)	RPS7 (I45V)	Single nucleotide variant (missense variant)	Diamond-Blackfan anemia 8	GUncertain significance
Select item 1086706	NM_001011.4(RPS7):c.285C>T (p.Ile95=)	RPS7	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia +1 more	GLikely benign
Select item 1064152	NM_001011.4(RPS7):c.357-3del	RPS7	Deletion (intron variant)	Diamond-Blackfan anemia 8	GUncertain significance
Select item 701700	NM_001011.4(RPS7):c.378C>T (p.His126=)	RPS7	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 8	GLikely benign

ClinVar