C0002726[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 364806	NM_198252.3(GSN):c.781G>A (p.Val261Ile)	GSN (V272I +7 more)	Single nucleotide variant (missense variant)	Meretoja syndrome +2 more	GUncertain significance
Select item 364834	NM_198252.3(GSN):c.*97GT[13]	GSN	Microsatellite (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364833	NM_198252.3(GSN):c.*97GT[12]	GSN	Microsatellite (3 prime UTR variant)	Amyloidosis	GBenign
Select item 364832	NM_198252.3(GSN):c.*97GT[11]	GSN	Microsatellite (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364831	NM_198252.3(GSN):c.97_98insGGTG	GSN	Insertion (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364836	NM_198252.3(GSN):c.116_117insGTG	GSN	Insertion (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364835	NM_198252.3(GSN):c.116_117insG	GSN	Insertion (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364837	NM_198252.3(GSN):c.120_121insG	GSN	Insertion (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364838	NM_198252.3(GSN):c.*136dup	GSN	Duplication (3 prime UTR variant)	Amyloidosis	GUncertain significance
Select item 364839	NM_198252.3(GSN):c.124_125insC	GSN	Insertion (3 prime UTR variant)	Amyloidosis	GUncertain significance