List of variants in gene CTNS reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_004937.3(CTNS):c.682-98G>A	rs112318471	0.02977
NM_004937.3(CTNS):c.852+275C>T	rs143878662	0.01069
NM_004937.3(CTNS):c.226-194G>A	rs116061320	0.00696
NM_004937.3(CTNS):c.108C>T (p.Asn36=)	rs117404824	0.00664
NM_004937.3(CTNS):c.853-28C>T	rs78671385	0.00563
NM_004937.3(CTNS):c.462-7C>A	rs189632527	0.00259
NM_004937.3(CTNS):c.116C>T (p.Ser39Leu)	rs144751390	0.00219
NM_004937.3(CTNS):c.971-114G>A	rs138808519	0.00192
NM_004937.3(CTNS):c.226-11C>T
NM_004937.3(CTNS):c.681+293_681+299del	rs11280317
NM_004937.3(CTNS):c.682-66C>A	rs111526586
NM_004937.3(CTNS):c.837C>T (p.Val279=)	rs779909823
NM_004937.3(CTNS):c.853-236G>A	rs79999227

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