Variants in gene PRX 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_181882.3(PRX):c.445G>A (p.Ala149Thr)	rs142436391	0.00193
NM_181882.3(PRX):c.3373G>A (p.Gly1125Ser)	rs148939995	0.00191
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys)	rs147587689	0.00185
NM_181882.3(PRX):c.3947C>T (p.Ala1316Val)	rs142762689	0.00138
NM_181882.3(PRX):c.1574T>C (p.Val525Ala)	rs149715830	0.00136
NM_181882.3(PRX):c.3838G>C (p.Glu1280Gln)	rs146205352	0.00135
NM_181882.3(PRX):c.823C>A (p.Leu275Ile)	rs200033507	0.00108
NM_181882.3(PRX):c.3110A>G (p.Glu1037Gly)	rs148600818	0.00099
NM_181882.3(PRX):c.3496C>T (p.Pro1166Ser)	rs147826200	0.00093
NM_181882.3(PRX):c.2548C>G (p.Pro850Ala)	rs141686828	0.00078
NM_181882.3(PRX):c.2164A>G (p.Met722Val)	rs376309142	0.00005
NM_181882.3(PRX):c.1222C>T (p.Pro408Ser)	rs150244426	0.00004

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