List of variants in gene GNS 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_002076.4(GNS):c.198G>A (p.Pro66=)	rs1147096	0.70681
NM_002076.4(GNS):c.*380C>T	rs674	0.63058
NM_002076.4(GNS):c.*2361C>G	rs1061743	0.52503
NM_002076.4(GNS):c.*1353G>A	rs1269548	0.51078
NM_002076.4(GNS):c.*269C>T	rs2279597	0.21062
NM_002076.4(GNS):c.363G>A (p.Lys121=)	rs2230291	0.09139
NM_002076.4(GNS):c.*942A>G	rs12309081	0.06453
NM_002076.4(GNS):c.*411G>A	rs11175525	0.06452
NM_002076.4(GNS):c.*1990A>G	rs17100600	0.04306
NM_002076.4(GNS):c.*566A>G	rs17100604	0.04303
NM_002076.4(GNS):c.1650T>C (p.His550=)	rs2230292	0.03695
NM_002076.4(GNS):c.*1456C>T	rs144199387	0.01725
NM_002076.4(GNS):c.459+14T>C	rs78614637	0.01673
NM_002076.4(GNS):c.21C>G (p.Ala7=)	rs61743823	0.00937
NM_002076.4(GNS):c.1598G>A (p.Arg533His)	rs61743822	0.00929
NM_002076.4(GNS):c.*814T>C	rs78614043	0.00798
NM_002076.4(GNS):c.*1228C>T	rs115625510	0.00797
NM_002076.4(GNS):c.*1648C>T	rs75568735	0.00795

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