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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_025132.4(WDR19):c.2792A>C (p.Tyr931Ser)	rs187546086	0.00261
NM_025132.4(WDR19):c.2702A>G (p.Tyr901Cys)	rs76326086	0.00108
NM_025132.4(WDR19):c.2715G>A (p.Lys905=)	rs200339331	0.00099
NM_025132.4(WDR19):c.2386G>A (p.Ala796Thr)	rs187332731	0.00095
NM_025132.4(WDR19):c.2364-3del	rs757992911	0.00079
NM_025132.4(WDR19):c.1198C>T (p.Leu400=)	rs199765304	0.00071
NM_025132.4(WDR19):c.2608G>A (p.Asp870Asn)	rs201963605	0.00064
NM_025132.4(WDR19):c.2671C>T (p.His891Tyr)	rs200266424	0.00062
NM_025132.4(WDR19):c.3008A>G (p.Glu1003Gly)	rs201354264	0.00056
NM_025132.4(WDR19):c.1248T>C (p.Asn416=)	rs772867899	0.00003
NM_025132.4(WDR19):c.2362G>A (p.Ala788Thr)	rs768082694	0.00003
NM_025132.4(WDR19):c.553C>G (p.Gln185Glu)	rs769602871

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