List of variants in gene WDR35 reported as uncertain significance for not specified

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.355C>T (p.Arg119Cys)	rs140308808	0.00221
NM_020779.4(WDR35):c.2066G>A (p.Arg689His)	rs74470618	0.00168
NM_020779.4(WDR35):c.1248T>G (p.Ile416Met)	rs144701688	0.00145
NM_020779.4(WDR35):c.3335A>G (p.Lys1112Arg)	rs138007924	0.00097
NM_020779.4(WDR35):c.2964+10C>A	rs201207790	0.00030
NM_020779.4(WDR35):c.2164C>T (p.Arg722Cys)	rs374073530	0.00011
NM_020779.4(WDR35):c.1376G>A (p.Arg459Gln)	rs146380332	0.00006
NM_020779.4(WDR35):c.1435A>G (p.Met479Val)	rs797046099	0.00002
NM_020779.4(WDR35):c.3495C>A (p.Cys1165Ter)	rs1475940439

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