C5568138[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1192585	NM_001199563.2(BVES):c.*114G>A	BVES	Single nucleotide variant (3 prime UTR variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X +1 more	GBenign
Select item 1192586	NM_001199563.2(BVES):c.351+30T>G	BVES	Single nucleotide variant (intron variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X +1 more	GBenign
Select item 1192587	NM_001199563.2(BVES):c.227-23G>A	BVES	Single nucleotide variant (intron variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X +1 more	GBenign

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