List of variants in gene PDSS2 reported as uncertain significance by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020381.4(PDSS2):c.667G>A (p.Val223Ile)	rs35555197	0.00130
NM_020381.4(PDSS2):c.1146G>A (p.Ser382=)	rs192206443	0.00022
NM_020381.4(PDSS2):c.908A>G (p.Glu303Gly)	rs545787240	0.00017
NM_020381.4(PDSS2):c.290C>T (p.Thr97Ile)
NM_020381.4(PDSS2):c.31C>T (p.Pro11Ser)

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