List of variants in gene WDR19 reported as likely pathogenic 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_025132.4(WDR19):c.3533G>A (p.Arg1178Gln)	rs79436363	0.00015
NM_025132.4(WDR19):c.3565+1G>A	rs587777352	0.00003
NM_025132.4(WDR19):c.275T>G (p.Leu92Ter)	rs926405916	0.00001
NM_025132.4(WDR19):c.142dup (p.Arg48fs)	rs1577823005
NM_025132.4(WDR19):c.3184-2A>C	rs1020915921
NM_025132.4(WDR19):c.617T>C (p.Leu206Pro)	rs1064796986
NM_025132.4(WDR19):c.728G>T (p.Gly243Val)	rs776687469
NM_025132.4(WDR19):c.742G>A (p.Gly248Ser)	rs1064796985

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