"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LRRC30"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2648554	NM_001105581.3(LRRC30):c.753C>G (p.Leu251=)	LRRC30	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1711456	GRCh37/hg19 18p11.32-11.22(chr18:1-8638260)x1	ADCYAP1, AKAIN1 +29 more	Copy number loss	not provided	GPathogenic
Select item 1701345	GRCh37/hg19 18p11.32-11.21(chr18:47390-14854037)x3	ADCYAP1, AFG3L2 +65 more	Copy number gain	not provided	GPathogenic

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