List of variants in gene PRX reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys)	rs147587689	0.00185
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.3186G>T (p.Lys1062Asn)	rs139188673	0.00105
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.862G>A (p.Val288Met)	rs568618329	0.00009
NM_181882.3(PRX):c.4307G>A (p.Arg1436Gln)	rs368827070	0.00006
NM_181882.3(PRX):c.3239G>A (p.Arg1080His)	rs762213719	0.00005
NM_181882.3(PRX):c.1391G>A (p.Arg464Gln)	rs553211374	0.00004
NM_181882.3(PRX):c.3646G>A (p.Val1216Met)	rs774413102	0.00002
NM_181882.3(PRX):c.994A>G (p.Thr332Ala)	rs143710873	0.00001
NM_181882.3(PRX):c.2230G>A (p.Glu744Lys)	rs2145728884
NM_181882.3(PRX):c.381+41G>A
NM_181882.3(PRX):c.7G>A (p.Ala3Thr)

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