C5676914[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1241806	NM_018082.6(POLR3B):c.72+184_72+188del	POLR3B	Deletion (5 prime UTR variant +1 more)	Charcot-Marie-Tooth disease, demyelinating, IIA 1I +3 more	GBenign
Select item 306930	NM_018082.6(POLR3B):c.773A>C (p.Glu258Ala)	POLR3B (E258A +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 1275967	NM_018082.6(POLR3B):c.1102-4_1102-3dup	POLR3B	Duplication (intron variant)	not provided +3 more	GBenign
Select item 1241049	NM_018082.6(POLR3B):c.1102-3dup	POLR3B	Duplication (intron variant)	Charcot-Marie-Tooth disease, demyelinating, IIA 1I +3 more	GBenign
Select item 488794	NM_018082.6(POLR3B):c.1263+2T>C	POLR3B	Single nucleotide variant (splice donor variant)	Charcot-Marie-Tooth disease, demyelinating, IIA 1I +4 more	GPathogenic/Likely pathogenic
Select item 31166	NM_018082.6(POLR3B):c.1568T>A (p.Val523Glu)	POLR3B (V523E +1 more)	Single nucleotide variant (missense variant)	not specified +8 more	GPathogenic/Likely pathogenic

ClinVar