Variants in gene WDR19 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025132.4(WDR19):c.3250G>A (p.Gly1084Ser)	rs16995209	0.03548
NM_025132.4(WDR19):c.1357-10T>C	rs16995189	0.01827
NM_025132.4(WDR19):c.2792A>C (p.Tyr931Ser)	rs187546086	0.00275
NM_025132.4(WDR19):c.-15G>T	rs150860929	0.00252
NM_025132.4(WDR19):c.3183+9G>A	rs138318063	0.00248
NM_025132.4(WDR19):c.2142+12G>A	rs149621476	0.00246
NM_025132.4(WDR19):c.2361C>T (p.Phe787=)	rs200133722	0.00165
NM_025132.4(WDR19):c.3416A>G (p.Gln1139Arg)	rs75621037	0.00065
NM_025132.4(WDR19):c.3249T>C (p.Asp1083=)	rs371128500	0.00034
NM_025132.4(WDR19):c.1595T>C (p.Ile532Thr)	rs749672769	0.00019
NM_025132.4(WDR19):c.3027C>T (p.Asp1009=)	rs181975379	0.00011
NM_025132.4(WDR19):c.2151G>A (p.Glu717=)	rs747574122	0.00008
NM_025132.4(WDR19):c.2454C>T (p.Ala818=)	rs748535483	0.00008
NM_025132.4(WDR19):c.3722C>T (p.Pro1241Leu)	rs576113399	0.00003
NM_025132.4(WDR19):c.916T>C (p.Leu306=)	rs757561646	0.00002

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.