"Illumina Laboratory Services, Illumina"[submitter] AND "LOC121587601" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 324047	NM_000023.4(SGCA):c.*90A>G	LOC121587601, SGCA	Single nucleotide variant (3 prime UTR variant +1 more)	Sarcoglycanopathy	GUncertain significance
Select item 324048	NM_000023.4(SGCA):c.*92C>T	LOC121587601, SGCA	Single nucleotide variant (3 prime UTR variant +1 more)	Sarcoglycanopathy	GBenign
Select item 324049	NM_000023.4(SGCA):c.*134del	LOC121587601, SGCA	Deletion (3 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 324050	NM_000023.4(SGCA):c.*148G>A	LOC121587601, SGCA	Single nucleotide variant (3 prime UTR variant +1 more)	Sarcoglycanopathy	GUncertain significance
Select item 324051	NM_000023.4(SGCA):c.*166A>G	LOC121587601, SGCA	Single nucleotide variant (3 prime UTR variant +1 more)	Sarcoglycanopathy	GBenign
Select item 324052	NM_000023.4(SGCA):c.*227G>A	LOC121587601, SGCA	Single nucleotide variant (3 prime UTR variant +1 more)	Sarcoglycanopathy	GUncertain significance

ClinVar