"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LSP1"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2641351	NM_002339.3(LSP1):c.654C>A (p.Ser218=)	LSP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024836	NM_001395380.1(PRR33):c.1412G>A (p.Arg471His)	LSP1, PRR33 (R471H)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2641352	NM_001395380.1(PRR33):c.15T>C (p.Ala5=)	LSP1, PRR33	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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