"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LRRC14"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658997	NM_001024678.4(LRRC24):c.1113G>A (p.Gln371=)	LOC130001413, LRRC14 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658998	NM_001024678.4(LRRC24):c.837T>A (p.Val279=)	LRRC14, LRRC24	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	LY6E, LY6H +173 more	Copy number gain	not provided	GPathogenic

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