List of variants in gene ALX4 reported as uncertain significance by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_021926.4(ALX4):c.917C>T (p.Pro306Leu)	rs149897209	0.00052
NM_021926.4(ALX4):c.627C>A (p.Ser209Arg)	rs568863681	0.00008
NM_021926.4(ALX4):c.596C>T (p.Pro199Leu)	rs758249273	0.00002
NM_021926.4(ALX4):c.648G>A (p.Arg216=)	rs550698378	0.00002
NM_021926.4(ALX4):c.171C>A (p.Phe57Leu)	rs1956497098	0.00001
NM_021926.4(ALX4):c.730C>T (p.Arg244Trp)	rs1167159867	0.00001
NM_021926.4(ALX4):c.1089C>A (p.His363Gln)
NM_021926.4(ALX4):c.166G>A (p.Gly56Arg)	rs2119925413
NM_021926.4(ALX4):c.772G>A (p.Val258Met)	rs747909089
NM_021926.4(ALX4):c.783G>T (p.Trp261Cys)	rs2539827537
NM_021926.4(ALX4):c.886C>T (p.Arg296Ter)	rs753073089
NM_021926.4(ALX4):c.901G>C (p.Ala301Pro)	rs766411205
NM_021926.4(ALX4):c.994A>C (p.Met332Leu)	rs1956205464

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