"GeneDx"[submitter] AND "LMOD2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152912	GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3	AASS, ABCB8 +1547 more	Copy number gain	See cases	GPathogenic
Select item 144923	GRCh38/hg38 7q31.32-31.33(chr7:123319393-124170657)x3	ASB15, ASB15-AS1 +20 more	Copy number gain	See cases	GUncertain significance
Select item 1232723	NM_207163.3(LMOD2):c.-54C>T	LMOD2	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1236647	NM_207163.3(LMOD2):c.273+30C>A	LMOD2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279919	NM_207163.3(LMOD2):c.274-107T>A	LMOD2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263755	NM_207163.3(LMOD2):c.300A>G (p.Glu100=)	LMOD2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1235659	NM_207163.3(LMOD2):c.1617+220A>G	LMOD2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253455	GRCh37/hg19 7q31.1-32.1(chr7:111613396-127897316)x1	AASS, RNU2-1 +57 more	Copy number loss	See cases	GPathogenic

ClinVar