Variants in gene WDR35 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val)	rs148242353	0.00233
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.2678T>C (p.Leu893Ser)	rs151047156	0.00093
NM_020779.4(WDR35):c.3467T>G (p.Ile1156Arg)	rs147325795	0.00072
NM_020779.4(WDR35):c.1227A>G (p.Thr409=)	rs148828104	0.00059
NM_020779.4(WDR35):c.1072G>A (p.Val358Ile)	rs151227688	0.00051
NM_020779.4(WDR35):c.1051C>G (p.Pro351Ala)	rs140753861	0.00045
NM_020779.4(WDR35):c.3252G>A (p.Glu1084=)	rs182360785	0.00014
NM_020779.4(WDR35):c.2777A>G (p.Tyr926Cys)	rs75602337	0.00013
NM_020779.4(WDR35):c.2109T>G (p.Thr703=)	rs201822027	0.00008

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