List of variants in gene combination LOC126863256, WDR45 reported as likely benign 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001029896.2(WDR45):c.235+364C>T	rs143453364	0.00380
NM_001029896.2(WDR45):c.-17-19T>G	rs371546812	0.00082
NM_001029896.2(WDR45):c.100G>A (p.Val34Met)	rs151051355	0.00010
NM_001029896.2(WDR45):c.-12C>T	rs782603489	0.00002
NM_001029896.2(WDR45):c.135C>T (p.His45=)	rs782629776	0.00002
NM_001029896.2(WDR45):c.20G>A (p.Arg7Gln)	rs782671518	0.00002
NM_001029896.2(WDR45):c.-17-15C>T	rs1557084580
NM_001029896.2(WDR45):c.131-7T>C	rs1057524035
NM_001029896.2(WDR45):c.56-12T>A	rs782407000

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