List of variants in gene SELENON reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_020451.3(SELENON):c.*1722T>C	rs4659383	0.80506
NM_020451.3(SELENON):c.425G>A (p.Cys142Tyr)	rs7349185	0.78899
NM_020451.3(SELENON):c.1173T>C (p.Pro391=)	rs760597	0.73933
NM_020451.3(SELENON):c.*1612T>C	rs3203750	0.70822
NM_020451.3(SELENON):c.1506C>A (p.Asn502Lys)	rs2294228	0.64022
NM_020451.3(SELENON):c.*2465G>A	rs6872	0.16329
NM_020451.3(SELENON):c.981C>T (p.Arg327=)	rs147587542	0.02788
NM_020451.3(SELENON):c.*144C>G	rs58895091	0.02379
NM_020451.3(SELENON):c.1745G>A (p.Arg582Gln)	rs74060854	0.02376
NM_020451.3(SELENON):c.*2043G>T	rs74060855	0.02333
NM_020451.3(SELENON):c.42C>T (p.Pro14=)	rs187960531	0.02295
NM_020451.3(SELENON):c.1387+11C>T	rs59653066	0.01839
NM_020451.3(SELENON):c.*1500G>A	rs116792929	0.01369
NM_020451.3(SELENON):c.409A>G (p.Thr137Ala)	rs35019869	0.01231
NM_020451.3(SELENON):c.*501G>A	rs112884056	0.00998
NM_020451.3(SELENON):c.*228C>T	rs115473437	0.00976
NM_020451.3(SELENON):c.*698T>C	rs147807764	0.00671
NM_020451.3(SELENON):c.1645G>A (p.Val549Met)	rs147131452	0.00268
NM_020451.3(SELENON):c.*2130C>T	rs79324169	0.00164
NM_020451.3(SELENON):c.1092+6C>G	rs148071754

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