List of variants in gene PDSS2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_020381.4(PDSS2):c.667G>A (p.Val223Ile)	rs35555197	0.00123
NM_020381.4(PDSS2):c.1046G>A (p.Arg349Gln)	rs201388841	0.00027
NM_020381.4(PDSS2):c.376A>G (p.Ser126Gly)	rs200386735	0.00009
NM_020381.4(PDSS2):c.50C>T (p.Ser17Leu)	rs373021095	0.00009
NM_020381.4(PDSS2):c.332T>C (p.Leu111Ser)	rs2115246578	0.00001
NM_020381.4(PDSS2):c.1169A>G (p.Asn390Ser)
NM_020381.4(PDSS2):c.154G>A (p.Val52Ile)	rs1282869756
NM_020381.4(PDSS2):c.378C>G (p.Ser126Arg)	rs1562468628
NM_020381.4(PDSS2):c.872A>G (p.His291Arg)	rs766749567
NM_020381.4(PDSS2):c.941A>C (p.Asn314Thr)	rs148925842

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