C3554042[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 945300	NM_000987.5(RPL26):c.377G>A (p.Arg126His)	RPL26 (R126H)	Single nucleotide variant (missense variant)	Diamond-Blackfan anemia 11 +2 more	GUncertain significance
Select item 704376	NM_000987.5(RPL26):c.342C>T (p.Asp114=)	RPL26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia +1 more	GLikely benign
Select item 1164657	NM_000987.5(RPL26):c.327A>G (p.Leu109=)	RPL26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 11 +1 more	GBenign/Likely benign
Select item 1634626	NM_000987.5(RPL26):c.168+17G>A	RPL26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 11 +1 more	GBenign/Likely benign
Select item 463369	NM_000987.5(RPL26):c.96C>T (p.Ser32=)	RPL26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 11 +1 more	GBenign/Likely benign
Select item 514617	NM_000987.5(RPL26):c.-5-16_-5-15del	RPL26	Deletion (intron variant)	Diamond-Blackfan anemia 11 +1 more	GBenign/Likely benign

ClinVar