"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SNHG22"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1626596	NM_001080467.3(MYO5B):c.4764C>T (p.Thr1588=)	MYO5B, SNHG22	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 711603	NM_001080467.3(MYO5B):c.4481C>T (p.Ser1494Leu)	MYO5B, SNHG22 (S1494L)	Single nucleotide variant (missense variant)	Cholestasis, progressive familial intrahepatic, 10 +2 more	GBenign/Likely benign