List of variants in gene WDR19 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_025132.4(WDR19):c.910G>A (p.Val304Ile)	rs75964850	0.03961
NM_025132.4(WDR19):c.3667C>T (p.Arg1223Cys)	rs201597047	0.00150
NM_025132.4(WDR19):c.3416A>G (p.Gln1139Arg)	rs75621037	0.00065
NM_025132.4(WDR19):c.3008A>G (p.Glu1003Gly)	rs201354264	0.00056
NM_025132.4(WDR19):c.2329A>G (p.Ile777Val)	rs373737104	0.00013
NM_025132.4(WDR19):c.2632C>T (p.Arg878Cys)	rs770091572	0.00003
NM_025132.4(WDR19):c.3722C>T (p.Pro1241Leu)	rs576113399	0.00003
NM_025132.4(WDR19):c.1931C>T (p.Thr644Met)	rs770339514	0.00002
NM_025132.4(WDR19):c.1629A>G (p.Pro543=)	rs776659376	0.00001
NM_025132.4(WDR19):c.3565C>T (p.His1189Tyr)	rs778261943	0.00001
NM_025132.4(WDR19):c.389G>A (p.Arg130Gln)	rs747065633	0.00001
NM_025132.4(WDR19):c.1099C>G (p.Leu367Val)	rs1064797308
NM_025132.4(WDR19):c.1746C>T (p.Tyr582=)
NM_025132.4(WDR19):c.2378A>C (p.Asn793Thr)
NM_025132.4(WDR19):c.3918C>T (p.Ile1306=)

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