List of variants in gene WDR35 reported as pathogenic for not provided

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.1889T>G (p.Leu630Ter)	rs199952377	0.00019
NM_020779.4(WDR35):c.1255+1G>A	rs371669862	0.00004
NM_020779.4(WDR35):c.2998G>T (p.Glu1000Ter)	rs886043316
NM_020779.4(WDR35):c.570+1G>C	rs2103456695
NM_020779.4(WDR35):c.707G>A (p.Cys236Tyr)	rs1672141593

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