List of variants in gene HGSNAT reported as likely 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_152419.3(HGSNAT):c.1567A>C (p.Lys523Gln)	rs73569592	0.03631
NM_152419.3(HGSNAT):c.*817C>T	rs78952714	0.01352
NM_152419.3(HGSNAT):c.*3213T>A	rs141634395	0.00899
NM_152419.3(HGSNAT):c.1693G>C (p.Gly565Arg)	rs148632988	0.00633
NM_152419.3(HGSNAT):c.*2258A>G	rs78930544	0.00584
NM_152419.3(HGSNAT):c.*2767C>T	rs74762381	0.00479
NM_152419.3(HGSNAT):c.1250+7G>A	rs74795999	0.00475
NM_152419.3(HGSNAT):c.1843G>A (p.Ala615Thr)	rs112029032	0.00361
NM_152419.3(HGSNAT):c.*2740C>T	rs114940430	0.00314
NM_152419.3(HGSNAT):c.*106G>A	rs186881132	0.00024
NM_152419.3(HGSNAT):c.1272C>T (p.Gly424=)	rs147251143	0.00019
NM_152419.3(HGSNAT):c.*2802C>G	rs187372766

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