List of variants in gene SAG reported as likely benign for retinal disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000541.5(SAG):c.375+11C>T	rs74356516	0.03568
NM_000541.5(SAG):c.201C>T (p.Cys67=)	rs72976383	0.02235
NM_000541.5(SAG):c.*89C>T	rs78338185	0.01526
NM_000541.5(SAG):c.1091C>T (p.Pro364Leu)	rs112613526	0.00622
NM_000541.5(SAG):c.301G>A (p.Ala101Thr)	rs141521563	0.00492
NM_000541.5(SAG):c.-69G>A	rs189763324	0.00397
NM_000541.5(SAG):c.588G>A (p.Ala196=)	rs190853693	0.00217
NM_000541.5(SAG):c.-223C>G	rs140569105	0.00170
NM_000541.5(SAG):c.420A>G (p.Pro140=)	rs150046934	0.00141
NM_000541.5(SAG):c.*90G>A	rs143418950

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